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Submitter
Lana Karapetyan1
Programme
Cancer Omics1
Creator
Arsen Arakelyan1
1
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Aligned sequencing data is available in the NCBI Sequence Read Archive (SRA, https://www.ncbi.nlm.nih.gov/sra/) under accession SRP095082. Variants were called using GATK HaplotypeCaller (version 3.6). After joint performing joint genotyping multi-sample vcf file was generated. Next, SNPs and indels were extracted into two different vcf files and specific set of filters were applied for each case.
Creator: Arsen Arakelyan
Submitter: Lana Karapetyan
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