ensembl-comparaThe Ensembl Compara Perl API and SQL schema
Stars: ✭ 43 (+115%)
BiopythonOfficial git repository for Biopython (originally converted from CVS)
Stars: ✭ 2,936 (+14580%)
SibeliazA fast whole-genome aligner based on de Bruijn graphs
Stars: ✭ 76 (+280%)
CAFE5Version 5 of the CAFE phylogenetics software
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TypeTEGenotyping of segregating mobile elements insertions
Stars: ✭ 15 (-25%)
SigProfilerExtractorSigProfilerExtractor allows de novo extraction of mutational signatures from data generated in a matrix format. The tool identifies the number of operative mutational signatures, their activities in each sample, and the probability for each signature to cause a specific mutation type in a cancer sample. The tool makes use of SigProfilerMatrixGen…
Stars: ✭ 86 (+330%)
crazydocRead DNA sequences from colourful Microsoft Word documents
Stars: ✭ 18 (-10%)
reg-genRegulatory Genomics Toolbox: Python library and set of tools for the integrative analysis of high throughput regulatory genomics data.
Stars: ✭ 64 (+220%)
RcpiMolecular informatics toolkit with a comprehensive integration of bioinformatics and cheminformatics tools for drug discovery.
Stars: ✭ 22 (+10%)
matamMapping-Assisted Targeted-Assembly for Metagenomics
Stars: ✭ 18 (-10%)
flexidotHighly customizable, ambiguity-aware dotplots for visual sequence analyses
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blogsJupyter notebooks that support my graph data science blog posts at https://bratanic-tomaz.medium.com/
Stars: ✭ 153 (+665%)
echolocatoRAutomated statistical and functional fine-mapping pipeline with extensive API access to datasets.
Stars: ✭ 13 (-35%)
cran-network-structureScripts used for my UseR!2015 presentation on the network structure of CRAN
Stars: ✭ 22 (+10%)
CellOCellO: Gene expression-based hierarchical cell type classification using the Cell Ontology
Stars: ✭ 34 (+70%)
chromapFast alignment and preprocessing of chromatin profiles
Stars: ✭ 93 (+365%)
CAMSACAMSA: a tool for Comparative Analysis and Merging of Scaffold Assemblies
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geneviewGenomics data visualization in Python by using matplotlib.
Stars: ✭ 38 (+90%)
gencoreGenerate duplex/single consensus reads to reduce sequencing noises and remove duplications
Stars: ✭ 91 (+355%)
plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
Stars: ✭ 27 (+35%)
MSFraggerUltrafast, comprehensive peptide identification for mass spectrometry–based proteomics
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StackedDAEStacked Denoising AutoEncoder based on TensorFlow
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Graphs.jlAn optimized graphs package for the Julia programming language
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virnetVirNet: A deep attention model for viral reads identification
Stars: ✭ 26 (+30%)
bistroA library to build and execute typed scientific workflows
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ngstoolsMy own tools code for NGS data analysis (Next Generation Sequencing)
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picardmetrics🚦 Run Picard on BAM files and collate 90 metrics into one file.
Stars: ✭ 38 (+90%)
awesome-geneticsA curated list of awesome bioinformatics software.
Stars: ✭ 60 (+200%)
tiptoftPredict plasmids from uncorrected long read data
Stars: ✭ 27 (+35%)
block-alignerSIMD-accelerated library for computing global and X-drop affine gap penalty sequence-to-sequence or sequence-to-profile alignments using an adaptive block-based algorithm.
Stars: ✭ 58 (+190%)
wikicrushProcessor scripts for Wikipedia dumps to crush them into a dense binary format that is easy to pathfind with.
Stars: ✭ 46 (+130%)
netSmoothnetSmooth: A Network smoothing based method for Single Cell RNA-seq imputation
Stars: ✭ 23 (+15%)
snpsea📊 Identify cell types and pathways affected by genetic risk loci.
Stars: ✭ 26 (+30%)
epivizEpiViz is a scientific information visualization tool for genetic and epigenetic data, used to aid in the exploration and understanding of correlations between various genome features.
Stars: ✭ 65 (+225%)
perbasePer-base per-nucleotide depth analysis
Stars: ✭ 46 (+130%)
DSAData Structures and Algorithms
Stars: ✭ 13 (-35%)
AMIDDIntroduction to Applied Mathematics and Informatics in Drug Discovery (AMIDD)
Stars: ✭ 13 (-35%)
BioKEENA computational library for learning and evaluating biological knowledge graph embeddings
Stars: ✭ 41 (+105%)
SemiBinNo description or website provided.
Stars: ✭ 25 (+25%)
ccsCCS: Generate Highly Accurate Single-Molecule Consensus Reads (HiFi Reads)
Stars: ✭ 79 (+295%)
polyRADGenotype Calling with Uncertainty from Sequencing Data in Polyploids 🍌🍓🥔🍠🥝
Stars: ✭ 16 (-20%)
GenomicDataCommonsProvide R access to the NCI Genomic Data Commons portal.
Stars: ✭ 64 (+220%)
argo-graph-liteInteractive Graph Visualization in Your Browser
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bio toolsUseful bioinformatic scripts
Stars: ✭ 35 (+75%)
mcscanCommand-line program to wrap dagchainer and combine pairwise results into multi-alignments in column format
Stars: ✭ 18 (-10%)
SumStatsRehabGWAS summary statistics files QC tool
Stars: ✭ 19 (-5%)
Competitive-ProgrammingThis repo conatins the code of the problems practised by me on Codeforces,Codedchef,Leetcode,Geeks For Geeks
Stars: ✭ 14 (-30%)
referenceseekerRapid determination of appropriate reference genomes.
Stars: ✭ 65 (+225%)
Data-Structures-and-AlgorithmsImplementation of various Data Structures and algorithms - Linked List, Stacks, Queues, Binary Search Tree, AVL tree,Red Black Trees, Trie, Graph Algorithms, Sorting Algorithms, Greedy Algorithms, Dynamic Programming, Segment Trees etc.
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OpenGene.jl(No maintenance) OpenGene, core libraries for NGS data analysis and bioinformatics in Julia
Stars: ✭ 60 (+200%)
argparse2tooltransparently build CWL and Galaxy XML tool definitions for any script that uses argparse
Stars: ✭ 24 (+20%)
calourexploratory and interactive microbiome analyses based on heatmaps
Stars: ✭ 22 (+10%)
dna-sculpture3D printed sculpture of a DNA molecule, showing my own genome
Stars: ✭ 22 (+10%)