graphsimR package: Simulate Expression data from igraph network using mvtnorm (CRAN; JOSS)
Stars: ✭ 16 (-33.33%)
enformer-pytorchImplementation of Enformer, Deepmind's attention network for predicting gene expression, in Pytorch
Stars: ✭ 146 (+508.33%)
switchdeInference of switch-like differential expression along single-cell trajectories
Stars: ✭ 19 (-20.83%)
genoiseruse the noise
Stars: ✭ 15 (-37.5%)
vrs-pythonGA4GH Variation Representation Python Implementation
Stars: ✭ 35 (+45.83%)
gnomad-browserExplore gnomAD datasets on the web
Stars: ✭ 61 (+154.17%)
disqA library for manipulating bioinformatics sequencing formats in Apache Spark
Stars: ✭ 29 (+20.83%)
gubbinsRapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
Stars: ✭ 103 (+329.17%)
LRSDAYLRSDAY: Long-read Sequencing Data Analysis for Yeasts
Stars: ✭ 26 (+8.33%)
snp-sitesFinds SNP sites from a multi-FASTA alignment file
Stars: ✭ 182 (+658.33%)
human genomics pipelineA Snakemake workflow to process single samples or cohorts of paired-end sequencing data (WGS or WES) using trim galore/bwa/GATK4/parabricks.
Stars: ✭ 19 (-20.83%)
homerkitRead HOMER motif analysis output in R.
Stars: ✭ 13 (-45.83%)
mandrakeMandrake 🌿/👨🔬🦆 – Fast visualisation of the population structure of pathogens using Stochastic Cluster Embedding
Stars: ✭ 29 (+20.83%)
scarfToolkit for highly memory efficient analysis of single-cell RNA-Seq, scATAC-Seq and CITE-Seq data. Analyze atlas scale datasets with millions of cells on laptop.
Stars: ✭ 54 (+125%)
STingUltrafast sequence typing and gene detection from NGS raw reads
Stars: ✭ 15 (-37.5%)
psmcImplementation of the Pairwise Sequentially Markovian Coalescent (PSMC) model
Stars: ✭ 121 (+404.17%)
Clair3Clair3 - Symphonizing pileup and full-alignment for high-performance long-read variant calling
Stars: ✭ 119 (+395.83%)
pathfindRpathfindR: Enrichment Analysis Utilizing Active Subnetworks
Stars: ✭ 138 (+475%)
CUT-RUNTools-2.0CUT&RUN and CUT&Tag data processing and analysis
Stars: ✭ 36 (+50%)
fwdpy11Forward-time simulation in Python using fwdpp
Stars: ✭ 25 (+4.17%)
shell-genomicsIntroduction to the Command Line for Genomics
Stars: ✭ 54 (+125%)
samplePerforms memory-efficient reservoir sampling on very large input files delimited by newlines
Stars: ✭ 61 (+154.17%)
biopython-coronavirusBiopython Jupyter Notebook tutorial to characterize a small genome
Stars: ✭ 80 (+233.33%)
OpenOmicsA bioinformatics API and web-app to integrate multi-omics datasets & interface with public databases.
Stars: ✭ 22 (-8.33%)
phenolphenol: Phenotype ontology library
Stars: ✭ 15 (-37.5%)
CuteVCFsimple viewer for variant call format using htslib
Stars: ✭ 30 (+25%)
cryfaA secure encryption tool for genomic data
Stars: ✭ 53 (+120.83%)
bapBead-based single-cell atac processing
Stars: ✭ 20 (-16.67%)
instaGRAALLarge genome reassembly based on Hi-C data, continuation of GRAAL
Stars: ✭ 32 (+33.33%)
TangramSpatial alignment of single cell transcriptomic data.
Stars: ✭ 149 (+520.83%)
haslrA fast tool for hybrid genome assembly of long and short reads
Stars: ✭ 68 (+183.33%)
DGCADifferential Gene Correlation Analysis
Stars: ✭ 32 (+33.33%)
dorotheaR package to access DoRothEA's regulons
Stars: ✭ 98 (+308.33%)
DRAMDistilled and Refined Annotation of Metabolism: A tool for the annotation and curation of function for microbial and viral genomes
Stars: ✭ 159 (+562.5%)
haystack bioHaystack: Epigenetic Variability and Transcription Factor Motifs Analysis Pipeline
Stars: ✭ 42 (+75%)
mitymity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data
Stars: ✭ 27 (+12.5%)
atacrAnalysing Capture Seq Count Data
Stars: ✭ 14 (-41.67%)
biglya pileup library that embraces the huge
Stars: ✭ 38 (+58.33%)
assembly improvementImprove the quality of a denovo assembly by scaffolding and gap filling
Stars: ✭ 46 (+91.67%)
deepgoFunction prediction using a deep ontology-aware classifier
Stars: ✭ 65 (+170.83%)
bactmapA mapping-based pipeline for creating a phylogeny from bacterial whole genome sequences
Stars: ✭ 36 (+50%)
GNEThis repository contains the tensorflow implementation of "GNE: A deep learning framework for gene network inference by aggregating biological information"
Stars: ✭ 27 (+12.5%)
gawnGenome Annotation Without Nightmares
Stars: ✭ 35 (+45.83%)
SplitThreaderExplore rearrangements and copy-number amplifications in a cancer genome
Stars: ✭ 65 (+170.83%)
PHISTPhage-Host Interaction Search Tool
Stars: ✭ 19 (-20.83%)
ontobiopython library for working with ontologies and ontology associations
Stars: ✭ 104 (+333.33%)
simuGsimuG: a general-purpose genome simulator
Stars: ✭ 68 (+183.33%)
bfcHigh-performance error correction for Illumina resequencing data
Stars: ✭ 66 (+175%)
DISCOVERDISCOVER co-occurrence and mutual exclusivity analysis for cancer genomics data
Stars: ✭ 21 (-12.5%)
PECAPECA is a software for inferring context specific gene regulatory network from paired gene expression and chromatin accessibility data
Stars: ✭ 31 (+29.17%)
redundansRedundans is a pipeline that assists an assembly of heterozygous/polymorphic genomes.
Stars: ✭ 90 (+275%)