Illumina paired whole exome sequencing of Rare Pediatric Phonotypes Study patient s1

SRX309642 Familial_Exome_Seq_Rare_Pediatric_Phenotypes-1 Illumina paired whole exome sequencing of Rare Pediatric Phonotypes Study patient s1 SRP026145 phs000553 Whole exome target capture (Agilent SureSelect Human All Exon 38mb. Fragmentation was done with a Covaris ultrasonicator (E220). SRS449755 SAMN01906002 sequencing library-1 WXS GENOMIC other 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina Genome Analyzer IIx Novoalign SRX309643 Familial_Exome_Seq_Rare_Pediatric_Phenotypes-2 Illumina paired whole exome sequencing of Rare Pediatric Phonotypes Study patient s2 SRP026145 phs000553 Whole exome target capture (Agilent SureSelect Human All Exon 38mb. Fragmentation was done with a Covaris ultrasonicator (E220). SRS449756 SAMN01906001 sequencing library-2 WXS GENOMIC other 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina Genome Analyzer IIx Novoalign SRX309644 Familial_Exome_Seq_Rare_Pediatric_Phenotypes-3 Illumina paired whole exome sequencing of Rare Pediatric Phonotypes Study patient s3 SRP026145 phs000553 Whole exome target capture (Agilent SureSelect Human All Exon 38mb. Fragmentation was done with a Covaris ultrasonicator (E220). SRS449757 SAMN01906000 sequencing library-3 WXS GENOMIC other 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina Genome Analyzer IIx Novoalign SRX309645 Familial_Exome_Seq_Rare_Pediatric_Phenotypes-4 Illumina paired whole exome sequencing of Rare Pediatric Phonotypes Study patient s4 SRP026145 phs000553 Whole exome target capture (Agilent SureSelect Human All Exon 38mb. Fragmentation was done with a Covaris ultrasonicator (E220). SRS449758 SAMN01906003 sequencing library-4 WXS GENOMIC other 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina Genome Analyzer IIx Novoalign SRX309646 Familial_Exome_Seq_Rare_Pediatric_Phenotypes-5 Illumina paired whole exome sequencing of Rare Pediatric Phonotypes Study patient s5 SRP026145 phs000553 Whole exome target capture (Agilent SureSelect Human All Exon 38mb. Fragmentation was done with a Covaris ultrasonicator (E220). SRS449759 SAMN01905999 sequencing library-5 WXS GENOMIC other 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina Genome Analyzer IIx Novoalign SRX309647 Familial_Exome_Seq_Rare_Pediatric_Phenotypes-6 Illumina paired whole exome sequencing of Rare Pediatric Phonotypes Study patient s6 SRP026145 phs000553 Whole exome target capture (Agilent SureSelect Human All Exon 38mb. Fragmentation was done with a Covaris ultrasonicator (E220). SRS449761 SAMN01905998 sequencing library-6 WXS GENOMIC other 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina Genome Analyzer IIx Novoalign SRX309648 Familial_Exome_Seq_Rare_Pediatric_Phenotypes-7 Illumina paired whole exome sequencing of Rare Pediatric Phonotypes Study patient s7 SRP026145 phs000553 Whole exome target capture (Agilent SureSelect Human All Exon 38mb. Fragmentation was done with a Covaris ultrasonicator (E220). SRS449754 SAMN01905997 sequencing library-7 WXS GENOMIC other 150 0 Application Read Forward 1 1 Application Read Reverse 76 Illumina Genome Analyzer IIx Novoalign