JayP718 / powertable_bb_plugin

Related projects ⓘ

Alternatives and complementary repositories for powertable_bb_plugin

• phenotips / open-pedigree
  A free and open-source pedigree tool by PhenoTips®
  ☆46Updated 10 months ago
• shishenyxx / Adult_brain_somatic_mosaicism
  This repository collects pipelines, codes, and some intermediate results for adult brain somatic mosaicism study.
  ☆14Updated 5 months ago
• EBIvariation / vcf-validator
  Validation suite for Variant Call Format (VCF) files, implemented using C++11
  ☆131Updated last month
• odelaneau / shapeit4
  Segmented HAPlotype Estimation and Imputation Tool
  ☆90Updated last year
• LuyiTian / FLAMES
  Full-length transcriptome splicing and mutation analysis
  ☆73Updated 4 months ago
• TheJacksonLaboratory / IntroToHPC
  HPC and queue usage class syllabus
  ☆16Updated 3 years ago
• isglobal-brge / methylclock
  DNA methylation-based clocks
  ☆39Updated 11 months ago
• iobio / gene.iobio
  Gene.iobio vue
  ☆57Updated last week
• freeseek / mocha
  MOsaic CHromosomal Alterations (MoChA) caller
  ☆81Updated last month
• nf-core / crisprseq
  A pipeline for the analysis of CRISPR edited data. It allows the evaluation of the quality of gene editing experiments using targeted nex…
  ☆31Updated last week
• dieterich-lab / circtools
  circtools: a modular, python-based framework for circRNA-related tools that unifies several functionalities in a single, command line dri…
  ☆26Updated 11 months ago
• sib-swiss / NGS-variants-training
  GitHub for the SIB courses NGS - Genome variant analysis
  ☆25Updated 2 months ago
• Ensembl / ensembl-hive
  EnsEMBL Hive - a system for creating and running pipelines on a distributed compute resource
  ☆52Updated last month
• raphael-group / hatchet
  HATCHet (Holistic Allele-specific Tumor Copy-number Heterogeneity) is an algorithm that infers allele and clone-specific CNAs and WGDs jo…
  ☆69Updated last month
• ShixiangWang / DoAbsolute
  Automate Absolute Copy Number Calling using 'ABSOLUTE' package
  ☆37Updated 11 months ago
• fredhutchio / tfcb_2019
  class materials for MCB517A through UW/Fred Hutch
  ☆10Updated 4 years ago
• parklab / MuSiCal
  A comprehensive toolkit for mutational signature analysis
  ☆31Updated 4 months ago
• nf-core / mnaseseq
  MNase-seq analysis pipeline using BWA and DANPOS2.
  ☆10Updated 6 months ago
• vertgenlab / gonomics
  A collection of genomics software tools written in Go (golang).
  ☆81Updated this week
• cancerit / ascatNgs
  Somatic copy number analysis using WGS paired end wholegenome sequencing
  ☆69Updated 4 years ago
• Illumina / paragraph
  Graph realignment tools for structural variants
  ☆152Updated last year
• plantimals / 2vcf
  convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations
  ☆52Updated 5 years ago
• colomemaria / epiAneufinder
  R package to detect breakpoints and assign somies to scATAC-seq data
  ☆33Updated 2 months ago
• AI-sandbox / gnomix
  A fast, scalable, and accurate local ancestry method.
  ☆87Updated 4 months ago
• epam / pipeline-builder
  Pipeline Builder is a JavaScript library for visualizing and constructing bioinformatics workflows, using Workflow Description Language (…
  ☆55Updated 7 months ago
• nf-core / isoseq
  Genome annotation with PacBio Iso-Seq. Takes raw subreads as input, generate Full Length Non Chemiric (FLNC) sequences and produce a bed …
  ☆29Updated last month
• apriha / snps
  tools for reading, writing, merging, and remapping SNPs
  ☆100Updated 2 months ago
• ekg / fastahack
  utilities for indexing and sequence extraction from FASTA files
  ☆59Updated 3 years ago
• nf-core / airrflow
  B-cell and T-cell Adaptive Immune Receptor Repertoire (AIRR) sequencing analysis pipeline using the Immcantation framework
  ☆54Updated 3 weeks ago
• nf-core / circrna
  circRNA quantification, differential expression analysis and miRNA target prediction of RNA-Seq data
  ☆44Updated last month