SRX2313558 BI-50 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770960 SAMN05930393 BI-50 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313559 BI-52 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770959 SAMN05930394 BI-52 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313560 BI-53 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770961 SAMN05930395 BI-53 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313561 BI-54 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770962 SAMN05930396 BI-54 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313562 BI-55 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770964 SAMN05930397 BI-55 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313563 BI-56 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770963 SAMN05930398 BI-56 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313564 BI-5 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770966 SAMN05930399 BI-5 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313565 BI-6 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770965 SAMN05930400 BI-6 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313566 BI-48 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770967 SAMN05930391 BI-48 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313567 BI-49 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770968 SAMN05930392 BI-49 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313568 NBH-6 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770969 SAMN05930643 NBH-6 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313569 BP-32 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770970 SAMN05930428 BP-32 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313570 BP-31 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770971 SAMN05930427 BP-31 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313571 BP-34 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770972 SAMN05930430 BP-34 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313572 BP-33 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770973 SAMN05930429 BP-33 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313573 BP-29 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770974 SAMN05930424 BP-29 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313574 BP-28 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770975 SAMN05930423 BP-28 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313575 BP-30 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770976 SAMN05930426 BP-30 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313576 BP-2 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770977 SAMN05930425 BP-2 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313577 BP-27 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770978 SAMN05930422 BP-27 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313578 BP-26 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770979 SAMN05930421 BP-26 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313579 F-33 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770980 SAMN05930528 F-33 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313580 F-34 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770981 SAMN05930529 F-34 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313581 F-31 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770982 SAMN05930526 F-31 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313582 F-32 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770983 SAMN05930527 F-32 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313583 F-2 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770984 SAMN05930524 F-2 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313584 F-30 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770985 SAMN05930525 F-30 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313585 F-28 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770986 SAMN05930522 F-28 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313586 F-29 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770987 SAMN05930523 F-29 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313587 F-26 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770988 SAMN05930520 F-26 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313588 F-27 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770989 SAMN05930521 F-27 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313589 F-18 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770990 SAMN05930511 F-18 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313590 F-17 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770991 SAMN05930510 F-17 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313591 F-21 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770992 SAMN05930515 F-21 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313592 F-20 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770993 SAMN05930514 F-20 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313593 F-1 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770994 SAMN05930513 F-1 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313594 F-19 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770995 SAMN05930512 F-19 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313595 F-25 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770996 SAMN05930519 F-25 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313596 F-24 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770997 SAMN05930518 F-24 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313597 F-23 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770998 SAMN05930517 F-23 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313598 F-22 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1770999 SAMN05930516 F-22 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313599 BP-24 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771000 SAMN05930419 BP-24 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313600 BP-25 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771001 SAMN05930420 BP-25 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313601 BP-22 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771002 SAMN05930417 BP-22 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313602 BP-23 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771003 SAMN05930418 BP-23 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313603 BP-20 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771004 SAMN05930415 BP-20 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313604 BP-21 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771005 SAMN05930416 BP-21 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313605 BP-19 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771006 SAMN05930413 BP-19 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313606 BP-1 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771007 SAMN05930414 BP-1 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313607 BP-17 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771008 SAMN05930411 BP-17 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313608 BP-18 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771010 SAMN05930412 BP-18 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313609 F-45 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771009 SAMN05930537 F-45 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313610 F-44 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771011 SAMN05930536 F-44 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313611 F-47 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771012 SAMN05930539 F-47 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313612 F-46 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771013 SAMN05930538 F-46 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313613 F-41 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771014 SAMN05930533 F-41 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313614 F-40 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771015 SAMN05930532 F-40 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313615 F-43 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771016 SAMN05930535 F-43 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313616 F-42 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771017 SAMN05930534 F-42 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313617 F-39 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771018 SAMN05930531 F-39 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313618 F-35 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771019 SAMN05930530 F-35 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313619 BP-7 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771020 SAMN05930451 BP-7 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313620 BP-8 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771021 SAMN05930452 BP-8 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313621 F-49 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771022 SAMN05930540 F-49 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313622 F-4 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771023 SAMN05930541 F-4 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313623 F-50 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771024 SAMN05930542 F-50 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313624 F-51 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771025 SAMN05930543 F-51 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313625 F-52 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771026 SAMN05930544 F-52 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313626 F-53 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771027 SAMN05930545 F-53 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313627 F-54 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771028 SAMN05930546 F-54 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313628 F-5 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771029 SAMN05930547 F-5 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313629 F-6 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771030 SAMN05930548 F-6 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313630 F-7 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771031 SAMN05930549 F-7 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313631 NBH-47 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771032 SAMN05930637 NBH-47 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313632 NBH-48 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771033 SAMN05930638 NBH-48 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313633 F-9 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771034 SAMN05930551 F-9 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313634 F-8 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771035 SAMN05930550 F-8 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313635 NBH-18 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771036 SAMN05930606 NBH-18 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313636 NBH-17 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771037 SAMN05930605 NBH-17 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313637 NBH-16 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771038 SAMN05930604 NBH-16 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313638 NBH-14 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771039 SAMN05930603 NBH-14 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313639 NBH-13 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771040 SAMN05930602 NBH-13 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313640 NBH-12 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771041 SAMN05930601 NBH-12 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313641 NBH-11 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771042 SAMN05930600 NBH-11 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313642 NBH-10 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771043 SAMN05930599 NBH-10 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313643 BI-23 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771044 SAMN05930366 BI-23 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313644 BI-22 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771046 SAMN05930365 BI-22 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313645 BI-21 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771045 SAMN05930364 BI-21 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313646 BI-20 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771047 SAMN05930363 BI-20 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313647 BI-27 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771048 SAMN05930370 BI-27 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313648 BI-26 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771049 SAMN05930369 BI-26 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313649 BI-25 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771050 SAMN05930368 BI-25 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313650 BI-24 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771051 SAMN05930367 BI-24 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313651 NBH-49 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771052 SAMN05930639 NBH-49 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313652 NBH-4 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771053 SAMN05930640 NBH-4 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313653 NBH-56 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771054 SAMN05930641 NBH-56 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313654 NBH-5 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771055 SAMN05930642 NBH-5 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313655 BI-19 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771056 SAMN05930362 BI-19 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313656 BI-17 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771057 SAMN05930361 BI-17 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313657 NBH-8 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771058 SAMN05930645 NBH-8 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313658 NBH-9 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771059 SAMN05930646 NBH-9 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313659 BP-48 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771060 SAMN05930442 BP-48 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313660 BP-47 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771061 SAMN05930441 BP-47 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313661 BP-51 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771062 SAMN05930446 BP-51 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313662 BP-50 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771063 SAMN05930445 BP-50 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313663 BP-4 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771064 SAMN05930444 BP-4 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313664 BP-49 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771065 SAMN05930443 BP-49 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313665 BP-6 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771066 SAMN05930450 BP-6 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313666 BP-5 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771067 SAMN05930449 BP-5 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313667 BP-53 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771068 SAMN05930448 BP-53 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313668 BP-52 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771069 SAMN05930447 BP-52 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313669 NBH-7 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771070 SAMN05930644 NBH-7 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313670 BI-39 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771071 SAMN05930382 BI-39 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313671 BI-38 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771072 SAMN05930381 BI-38 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313672 BI-41 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771073 SAMN05930384 BI-41 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313673 BI-40 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771074 SAMN05930383 BI-40 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313674 BI-43 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771075 SAMN05930386 BI-43 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313675 BI-42 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771076 SAMN05930385 BI-42 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313676 BI-45 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771077 SAMN05930388 BI-45 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313677 BI-44 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771078 SAMN05930387 BI-44 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313678 BI-47 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771079 SAMN05930390 BI-47 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313679 BI-46 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771080 SAMN05930389 BI-46 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313680 NBH-19 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771081 SAMN05930607 NBH-19 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313681 NBH-1 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771082 SAMN05930608 NBH-1 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313682 NBH-22 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771083 SAMN05930611 NBH-22 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313683 NBH-23 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771084 SAMN05930612 NBH-23 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313684 NBH-20 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771085 SAMN05930609 NBH-20 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313685 NBH-21 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771086 SAMN05930610 NBH-21 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313686 NBH-26 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771087 SAMN05930615 NBH-26 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313687 NBH-27 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771088 SAMN05930616 NBH-27 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313688 NBH-24 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771089 SAMN05930613 NBH-24 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313689 NBH-25 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771090 SAMN05930614 NBH-25 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313690 BI-11 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771091 SAMN05930357 BI-11 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313691 BI-12 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771092 SAMN05930358 BI-12 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313692 BI-14 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771093 SAMN05930359 BI-14 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313693 BI-15 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771095 SAMN05930360 BI-15 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313694 F-13 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771094 SAMN05930506 F-13 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313695 BI-10 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771096 SAMN05930356 BI-10 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313696 BP-38 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771097 SAMN05930431 BP-38 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313697 BP-39 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771098 SAMN05930432 BP-39 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313698 BP-43 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771099 SAMN05930437 BP-43 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313699 BP-44 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771100 SAMN05930438 BP-44 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313700 BP-45 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771101 SAMN05930439 BP-45 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313701 BP-46 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771102 SAMN05930440 BP-46 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313702 BP-3 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771103 SAMN05930433 BP-3 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313703 BP-40 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771104 SAMN05930434 BP-40 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313704 BP-41 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771105 SAMN05930435 BP-41 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313705 BP-42 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771106 SAMN05930436 BP-42 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313706 F-14 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771107 SAMN05930507 F-14 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313707 BI-28 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771109 SAMN05930371 BI-28 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313708 BI-29 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771108 SAMN05930372 BI-29 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313709 BI-32 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771111 SAMN05930375 BI-32 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313710 BI-33 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771110 SAMN05930376 BI-33 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313711 BI-2 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771112 SAMN05930373 BI-2 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313712 BI-30 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771113 SAMN05930374 BI-30 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313713 BI-36 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771114 SAMN05930379 BI-36 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313714 BI-37 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771115 SAMN05930380 BI-37 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313715 BI-34 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771116 SAMN05930377 BI-34 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313716 BI-35 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771119 SAMN05930378 BI-35 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313717 NBH-29 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771118 SAMN05930618 NBH-29 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313718 NBH-28 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771117 SAMN05930617 NBH-28 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313719 NBH-30 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771120 SAMN05930620 NBH-30 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313720 NBH-2 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771121 SAMN05930619 NBH-2 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313721 NBH-32 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771122 SAMN05930622 NBH-32 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313722 NBH-31 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771123 SAMN05930621 NBH-31 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313723 NBH-34 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771124 SAMN05930624 NBH-34 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313724 NBH-33 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771127 SAMN05930623 NBH-33 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313725 NBH-36 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771125 SAMN05930626 NBH-36 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313726 NBH-35 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771126 SAMN05930625 NBH-35 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313727 BI-8 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771128 SAMN05930402 BI-8 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313728 BI-7 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771130 SAMN05930401 BI-7 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313729 F-15 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771131 SAMN05930508 F-15 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313730 F-16 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771129 SAMN05930509 F-16 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313731 BP-9 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771132 SAMN05930453 BP-9 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313732 F-10 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771133 SAMN05930503 F-10 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313733 F-11 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771135 SAMN05930504 F-11 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313734 F-12 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771134 SAMN05930505 F-12 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313735 BP-16 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771136 SAMN05930410 BP-16 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313736 BP-15 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771137 SAMN05930409 BP-15 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313737 BP-14 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771139 SAMN05930408 BP-14 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313738 BP-13 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771138 SAMN05930407 BP-13 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313739 BP-12 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771140 SAMN05930406 BP-12 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313740 BP-11 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771141 SAMN05930405 BP-11 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313741 BP-10 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771143 SAMN05930404 BP-10 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313742 BI-9 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771142 SAMN05930403 BI-9 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313743 NBH-37 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771144 SAMN05930627 NBH-37 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313744 NBH-38 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771145 SAMN05930628 NBH-38 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313745 NBH-43 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771146 SAMN05930633 NBH-43 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313746 NBH-44 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771147 SAMN05930634 NBH-44 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313747 NBH-45 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771148 SAMN05930635 NBH-45 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313748 NBH-46 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771150 SAMN05930636 NBH-46 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313749 NBH-39 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771149 SAMN05930629 NBH-39 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313750 NBH-40 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771151 SAMN05930630 NBH-40 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313751 NBH-41 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771152 SAMN05930631 NBH-41 WGS GENOMIC RANDOM Illumina HiSeq 2500 SRX2313752 NBH-42 SRP092392 PRJNA323589 Following extraction and quantification, genomic DNA was sheared to 500bp by sonication (Covaris E220). Sheared DNA was used to construct individually-indexed sequencing libraries using the NextFlex DNA sequencing kit (Bioo Scientific). Library insert sizes were determined by TapeStation (Agilent) using DNA high sensitivity ScreenTape, and libraries were quantified by Quant-iT PicoGreen (Life Technologies). Following quantification, libraries were normalized to a uniform concentration and 96 indexed libraries were pooled on an equal molar basis for sequencing. Library construction, quantification, normalization, and pooling were conducted utilizing a dual-hybrid Biomek FXp automated liquid handler (Beckman Coulter). SRS1771153 SAMN05930632 NBH-42 WGS GENOMIC RANDOM Illumina HiSeq 2500