Archives

Scalpel: Indel 变异鉴定工具,支持单样本、家庭样本以及正常和肿瘤对样本

标题:

Indel variant analysis of short-read sequencing data with Scalpel.

摘要:

As the second most common type of variation in the human genome, insertions and deletions (indels) have been linked to many diseases, but the discovery of indels of more than a few bases in size from short-read sequencing data remains challenging. Scalpel (http://scalpel.sourceforge.net) is […]