RCollins13
Ryan is an instructor at Dana-Farber Cancer Institute studying the role of germline genetics in cancer. For more info, visit www.ryanlcollins.com
Dana-Farber Cancer InstituteBoston, MA
Pinned Repositories
gatk-sv
A structural variation pipeline for short-read sequencing
10XWGS
Utilities for processing 10X linked-read WGS data
CNValue
Analysis of rare CNVs (work in progress)
CNView
Visualization and annotation of CNVs from population-scale whole-genome sequencing data
GenomicsToolbox
Toolbox of utility genomics scripts
HumanIdiogramLibrary
Resource of human chromosome schematics & images
oncomod
Analysis of germline modifiers of RAS oncogenes
RLCtools
R library of helper functions used across projects
WGD
A suite of tools to evaluate dosage in whole-genome sequencing libraries
rCNV2
Aggregation and analyses of rare CNVs across diseases
RCollins13's Repositories
RCollins13/HumanIdiogramLibrary
Resource of human chromosome schematics & images
RCollins13/CNView
Visualization and annotation of CNVs from population-scale whole-genome sequencing data
RCollins13/WGD
A suite of tools to evaluate dosage in whole-genome sequencing libraries
RCollins13/GenomicsToolbox
Toolbox of utility genomics scripts
RCollins13/CNValue
Analysis of rare CNVs (work in progress)
RCollins13/10XWGS
Utilities for processing 10X linked-read WGS data
RCollins13/oncomod
Analysis of germline modifiers of RAS oncogenes
RCollins13/gatk-sv
A structural variation pipeline for short-read sequencing
RCollins13/proactive_wgs
Code supporting the analysis of PROACTIVE WGS data
RCollins13/ras_germline_wgs
Study of germline risk for RAS-driven cancers
RCollins13/RLCtools
R library of helper functions used across projects