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dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
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Method Detail
Submitter Method Handle: FSA-LAB
Submitter Method ID: ILLUMINAWHOLEEXOME
Submitted method description:
Exome capture was performed using the TruSeq Exome Enrichment kit (Illumina, San Diego, CA, USA) as per the manufacturer?s instructions.
Samples were prepared as an Illumina sequencing library, and in the second step, the sequencing libraries were enriched for the desired target using the Illumina Exome Enrichment protocol.
Captured libraries were sequenced using Illumina HiSeq 2000 Sequencer, and the reads mapped against UCSC hg19 (http://genome.ucsc.edu/) by BWA (http://bio-bwa.sourceforge.net/).
The SNPs and Indels were detected by SAMTOOLS (http://samtools.sourceforge.net/).

This method was used in the following submission:

Submitter Handle Batch Type Submitter batch id Release build id
FSA-LAB Assay Exome_SNP_Discovery 151

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