VarScan: variant detection in massively parallel sequencing of individual and pooled samples
Summary: Massively parallel sequencing technologies hold incredible promise for the study of DNA sequence variation, particularly the identification of variants affecting human disease. The unprecedented throughput and relatively short read lengths of Roche/454, Illumina/Solexa, and other platforms...
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| Main Authors: | , , , , , , , , |
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| Format: | Text |
| Language: | English |
| Published: |
Oxford University Press
2009
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| Subjects: | |
| Online Access: | https://pmc.ncbi.nlm.nih.gov/articles/PMC2734323/ https://pubmed.ncbi.nlm.nih.gov/19542151 http://dx.doi.org/10.1093/bioinformatics/btp373 |
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