A protocol for applying low-coverage whole-genome sequencing data in structural variation studies

Description

STAR Protocols is an open access, peer-reviewed journal from Cell Press. We offer structured, transparent, accessible, and repeatable step-by-step experimental and computational protocols from all areas of life, health, earth and physical sciences.

Detecting structural variations with precise breakpoints using low

Shuhua Xu's research works Fudan University, Shanghai and other places

3. Raw data processing — Single-cell best practices

Structural Variation Identification in Breast Cancer with Whole

Issues with SARS-CoV-2 sequencing data - nCoV-2019 Genomic

PDF] A spectrum of free software tools for processing the VCF variant call format: vcflib, bio-vcf, cyvcf2, hts-nim and slivar

PDF) PGG.SV: a whole-genome-sequencing-based structural variant resource and data analysis platform

Issues with SARS-CoV-2 sequencing data - nCoV-2019 Genomic

Stacks: Stacks Manual

PDF) A protocol for applying low-coverage whole-genome sequencing data in structural variation studies

Qi LIU, PostDoc Position, Doctor of Philosophy, Fudan University, Shanghai

Enabling low-pass whole genome sequencing