SRX18549350 b9__a_10 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000272 SRS16016016 SAMN25040799 b9__a_10 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549351 b9__a_12 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000273 SRS16016017 SAMN25040922 b9__a_12 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549352 b9__a_23 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000282 SRS16016018 SAMN25040907 b9__a_23 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549353 b9__a_25 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000283 SRS16016019 SAMN25040822 b9__a_25 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549354 b9__a_26 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000284 SRS16016020 SAMN25040814 b9__a_26 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549355 b9__a_27 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000285 SRS16016021 SAMN25040829 b9__a_27 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549356 b9__a_28 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000286 SRS16016022 SAMN25040863 b9__a_28 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549357 b9__a_29 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000287 SRS16016023 SAMN25040862 b9__a_29 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549358 b9__a_31 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000288 SRS16016024 SAMN25040773 b9__a_31 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549359 b9__a_32 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000289 SRS16016025 SAMN25040774 b9__a_32 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549360 b9__a_33 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000290 SRS16016026 SAMN25040784 b9__a_33 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549361 b9__a_34 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000291 SRS16016027 SAMN25040758 b9__a_34 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549362 b9__a_13 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000274 SRS16016028 SAMN25040860 b9__a_13 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549363 b9__a_35 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000292 SRS16016029 SAMN25040749 b9__a_35 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549364 b9__a_36 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000293 SRS16016030 SAMN25040818 b9__a_36 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549365 b9__a_38 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000294 SRS16016031 SAMN25040790 b9__a_38 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549366 b9__a_39 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000295 SRS16016032 SAMN25040900 b9__a_39 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549367 b9__a_4 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000296 SRS16016033 SAMN25040802 b9__a_4 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549368 b9__a_14 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000275 SRS16016034 SAMN25040769 b9__a_14 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549369 b9__a_15 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000276 SRS16016035 SAMN25040881 b9__a_15 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549370 b9__a_17 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000277 SRS16016036 SAMN25040766 b9__a_17 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549371 b9__a_18 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000278 SRS16016037 SAMN25040824 b9__a_18 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549372 b9__a_2 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000279 SRS16016038 SAMN25040880 b9__a_2 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549373 b9__a_20 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000280 SRS16016039 SAMN25040891 b9__a_20 WGS GENOMIC RANDOM Illumina NovaSeq 6000 SRX18549374 b9__a_21 SRP334402 PRJNA758215 DNA was extracted in-house from multiple individuals (cultures) for nematode and tardigrade species, or from single specimens for all other taxa. For microfauna and mesofauna, the whole specimen was used for DNA extraction, while body parts of macrofauna were used. A non-destructive DNA extraction protocol was followed, according to Gilbert et al. (2007), except for Illumina batch 8 where the standard DNeasy Tissue Kit was used (Qiagen Inc.). Library preparations were performed in-house for earlier Illumina batches, and directly at Novogene from batch 7 onwards according to the NEBNext Ultra II DNA Library Prep Kit. Gilbert MTP, Moore W, Melchior L, Worobey M (2007) DNA Extraction from Dry Museum Beetles without Conferring External Morphological Damage. PLoS ONE 2(3): e272. doi:10.1371/journal.pone.0000281 SRS16016040 SAMN25040865 b9__a_21 WGS GENOMIC RANDOM Illumina NovaSeq 6000