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- W3039991480 abstract "Abstract Summary We present a new version of the popular somatic variant caller, Lancet, that supports the analysis of linked-reads sequencing data. By seamlessly integrating barcodes and haplotype read assignments within the colored De Bruijn graph local-assembly framework, Lancet computes a barcode-aware coverage and identifies variants that disagree with the local haplotype structure. Availability and Implementation Lancet is implemented in C++ and is available for academic and non-commercial research purposes as an open-source package at https://github.com/nygenome/lancet . Contact gnarzisi@nygenome.org" @default.
- W3039991480 created "2020-07-10" @default.
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- W3039991480 date "2020-07-06" @default.
- W3039991480 modified "2023-09-23" @default.
- W3039991480 title "Somatic variant analysis of linked-reads sequencing data with Lancet" @default.
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- W3039991480 doi "https://doi.org/10.1101/2020.07.04.158063" @default.
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