<p>Somatic variant analysis of linked-reads sequencing data with Lancet</p>

Giuseppe Narzisi; Rajeeva Musunuri; André Corvelo; Kanika Arora; Minita Shah; Jennifer Shelton; Michael Zody

doi:10.7490/f1000research.1117597.1

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Narzisi G, Musunuri R, Corvelo A et al. Somatic variant analysis of linked-reads sequencing data with Lancet [version 1; not peer reviewed]. F1000Research 2019, 8:1857 (poster) (https://doi.org/10.7490/f1000research.1117597.1)

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Somatic variant analysis of linked-reads sequencing data with Lancet

Giuseppe Narzisi¹, Rajeeva Musunuri, André Corvelo, Kanika Arora, Minita Shah, Jennifer Shelton, Michael Zody

Published 05 Nov 2019 (https://doi.org/10.7490/f1000research.1117597.1)

Author Affiliations

¹ New York Genome Center, USA

Copyright © 2019 Narzisi G et al. This is an open access work distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Published 05 Nov 2019

Somatic variant analysis of linked-reads sequencing data with Lancet
[version 1; not peer reviewed]

Giuseppe Narzisi¹, Rajeeva Musunuri, André Corvelo, Kanika Arora, Minita Shah, Jennifer Shelton, Michael Zody

Author Affiliations

¹ New York Genome Center, USA

Presented at

Genome Informatics 2019

Abstract

Competing Interests

No competing interests were disclosed

Keywords

DNA sequence assembly, variant calling, colored De Bruijn Graph, Next-Generation sequencing, Linked-Reads, Cancer Genomics

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