tahashmi's Stars
hail-is/hail
Cloud-native genomic dataframes and batch computing
pangenome/pggb
the pangenome graph builder
schneebergerlab/plotsr
Tool to plot synteny and structural rearrangements between genomes
PapenfussLab/gridss
GRIDSS: the Genomic Rearrangement IDentification Software Suite
lbcb-sci/racon
Ultrafast consensus module for raw de novo genome assembly of long uncorrected reads
hartwigmedical/hmftools
Various algorithms for analysing genomics data
LooseLab/readfish
CLI tool for flexible and fast adaptive sampling on ONT sequencers
ablab/IsoQuant
Transcript discovery and quantification with long RNA reads (Nanopores and PacBio)
nygenome/lancet
Microassembly based somatic variant caller for NGS data
hatchet/hatchet
Analyze graph/hierarchical performance data using pandas dataframes
KolmogorovLab/Severus
A tool for somatic structural variant calling using long reads
xjtu-omics/SVision
Detecting genome structural variants with deep learning in single molecule sequencing
friend1ws/nanomonsv
SV detection tool for nanopore sequence reads
antmicro/google-coral-baseboard
Antmicro's open hardware baseboard for the Google Coral i.MX8 + Edge TPU SoM
raphael-group/hatchet
HATCHet (Holistic Allele-specific Tumor Copy-number Heterogeneity) is an algorithm that infers allele and clone-specific CNAs and WGDs jointly across multiple tumor samples from the same patient, and that leverages the relationships between clones in these samples.
katerinakazantseva/strainy
Graph-based assembly phasing
antmicro/zynq-video-board
Open Hardware carrier board supporting modules with Zynq 7000 All Programmable SoC devices.
ICGC-TCGA-PanCancer/TumorType-WGS
Classifying tumor types based on Whole Genome Sequencing (WGS) data
djnavarro/arrow-user2022
Larger-Than-Memory Data Workflows with Apache Arrow
TheJacksonLaboratory/Picky
Structural Variants Pipeline for Long Reads
fulcrumgenomics/python-snakemake-template
A template repository for Snakemake pipepline(s) and a python command-line toolkit.
TheJacksonLaboratory/ChIA-PIPE
ChIA-PIPE: A fully automated pipeline for comprehensive ChIA-PET data analysis and visualization
snurk/sg_sandbox
Experimental String Graph construction and processing
asherliu/simd-x
SIMD-X: Programming and Processing of Graph Algorithms on GPUs [USENIX ATC '19]
aganezov/RCK
RCK: Reconstruction of clone- and haplotype-specific Cancer Karyotypes
Magdoll/MagPhase
Phasing for metagenomics using PacBio long reads
polyactis/Accucopy
Accucopy is a computational method that infers Allele-Specific Copy Number alterations from low-coverage low-purity tumor sequencing data.
raphael-group/hatchet-paper
Related to (Zaccaria and Raphael, 2018), the repository contains the simulated data, the results of all methods involved in the comparison, the results of HATCHet on the prostate and pancreas cancer datasets, and all data and analysis related to these last two cancer datasets.
PMBio/mb-nanopore-2022
Analysis code for publication "Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signature"
usnistgov/giab-pFDA-2nd-challenge
Code and intermediate data used to generate figures and results for the manuscript describing the challenge.