Topic

bioinformatics

Repositories (1466)

polyRAD
polyRAD lvclark R

Genotype Calling with Uncertainty from Sequencing Data in Polyploids ๐ŸŒ๐Ÿ“๐Ÿฅ”๐Ÿ ๐Ÿฅ

16
libdna
libdna kloetzl C

โ™ฅ Essential Functions for DNA Manipulation

16
neuroexpresso
neuroexpresso PavlidisLab R

:bar_chart: Gene expression in neuroexpresso database

15
DL-based-Tumor-Classification
DL-based-Tumor-Classification HHHit Python

Deep Learning Based Tumor Type Classification Using Gene Expression Data

15
BMI219-2017-ProteinFolding
BMI219-2017-ProteinFolding pfnet-research Python

UCSF BMI219 Deep Learning (2017), Coding example (Prediction of protein folding with RNN and CNN)

15
gtaxon
gtaxon shenwei356 Go

gTaxon - a fast cross-platform NCBI taxonomy data querying (gi2taxid, taxid2taxon, name2taxid, LCA) tool, with cmd client and REST API server for both...

15
EternaBrain
EternaBrain eternagame Python

Deep learning to solve RNA design puzzles

15
lexicon-mono-seq
lexicon-mono-seq IbrahimTanyalcin JavaScript

DOM Text Based Multiple Sequence Alignment Library

15
shark
shark AlgoLab C++

Mapping-free software for fishing relevant reads in an RNA-Seq sample

15
mapping-iterative-assembler
mapping-iterative-assembler mpieva C

Consensus calling (or "reference assisted assembly"), chiefly of ancient mitochondria

15
parseR
parseR anilchalisey R

parseR: Pipeline for rna-seq analysis in R

15
seave
seave KCCG HTML

Seave is a web platform that enables genetic variants to be easily filtered and annotated with in silico pathogenicity prediction scores and annotatio...

15
bcgTree
bcgTree molbiodiv Perl

Automatically calculate phylogenetic trees from bacterial core genes

15
CliHelpParser
CliHelpParser aCLImatise Python

Reads the output from CLI help commands, and generates machine readable schemas (CWL etc)

15
orange3-bioinformatics
orange3-bioinformatics biolab Python

๐ŸŠ๐Ÿ”ฌ Bioinformatics add-on for Orange3

15
DEcode
DEcode stasaki Jupyter Notebook

A prediction model for differential gene expression (DE) based on genome-wide regulatory interactions

15
GslCore
GslCore Amyris F#

Core library and basic plug-ins for the Amyris Genotype Specification Language (GSL) compiler.

15
workflows
workflows stjudecloud wdl

Bioinformatics workflows developed for and used on the St. Jude Cloud project.

15
TypeTE
TypeTE clemgoub Perl

Genotyping of segregating mobile elements insertions

15
rnftools
rnftools karel-brinda Python

RNF framework for NGS: simulation of reads, evaluation of mappers, conversion of RNF-compliant data.

14
bionode-fasta
bionode-fasta bionode JavaScript

Streamable FASTA parser.

14
miprimer
miprimer ujenjt CSS

Webapp for design DNA primers for miRNA qPCR process

14
nomie-docs
nomie-docs happydata HTML

Nomie Documentation Repo for docs.nomie.io

14
chise.js
chise.js iVis-at-Bilkent JavaScript

A web application to visualize and edit the pathway models represented by SBGN Process Description Notation

14
homerkit
homerkit slowkow R

Read HOMER motif analysis output in R.

14
BLSS
BLSS Binomica-Labs C#

A suite of unique bioinformatics tools for the brave explorer.

14
sistr_cmd
sistr_cmd phac-nml Python

SISTR (Salmonella In Silico Typing Resource) command-line tool

14
SigProfilerSimulator
SigProfilerSimulator AlexandrovLab Python

SigProfilerSimulator allows realistic simulations of mutational patterns and mutational signatures in cancer genomes. The tool can be used to simulate...

14
srijan-gsoc-2020
srijan-gsoc-2020 vermasrijan Jupyter Notebook

Healthcare-Researcher-Connector Package: Federated Learning tool for bridging the gap between Healthcare providers and researchers

14
RPharma2020
RPharma2020 leonjessen HTML

R/Pharma Conference 2020. Repository for the workshop "Artificial Neural Networks in R with Keras and TensorFlow" by Leon Eyrich Jessen

14
TensorFlow-DNNs-for-Predicting-DNA-Transcription-Factor-Binding
TensorFlow-DNNs-for-Predicting-DNA-Transcription-Factor-Binding drewwiens Python

Deep neural networks implemented in TensorFlow & Python for predicting whether transcription factors will bind to given DNA sequences

14
s3-rust-htslib-bam
s3-rust-htslib-bam brainstorm Rust

AWS lambda S3 + rust-htslib: A serverless bioinformatics example

14
Synopsys-Project-2017
Synopsys-Project-2017 minhoolee Jupyter Notebook

A deep learning based bioinformatics project on epigenetics in Type 2 Diabetes.

14
Managing_Your_Biological_Data_with_Python_3
Managing_Your_Biological_Data_with_Python_3 raymonwu Jupyter Notebook

<<Managing Your Biological Data with Python>> wirtten in Python 3

14
GMQL
GMQL DEIB-GECO Scala

GMQL - GenoMetric Query Language

14
npdtools
npdtools ablab

Natural Product Discovery tools -- a toolkit containing various pipelines for in silico analysis of natural product mass spectrometry data

14
hrpi
hrpi SGDDNB HTML

Rmarkdown / compiled html files for human reprogramming dataset analysis

14
FAMLI
FAMLI FredHutch Jupyter Notebook

Functional Analysis of Metagenomes by Likelihood Inference

14
vcf-rs
vcf-rs informationsea Rust

Rust implmentation of VCF parser

14
RNAlien
RNAlien eggzilla Haskell

RNAlien - unsupervised RNA family model construction

13
genome_collector
genome_collector Edinburgh-Genome-Foundry Python

:stars: Easily download genomes and build BLAST/Bowtie indexes in Python

13
looper
looper pepkit Python

A job submitter for Portable Encapsulated Projects

13
atacr
atacr TeamMacLean R

Analysing Capture Seq Count Data

13
wort
wort sourmash-bio Python
13
azure-hpc
azure-hpc Azure JavaScript

Microsoft Azure HPC & Big Compute

13
physlr
physlr bcgsc Python

:chains: Construct a Physical Map from Linked Reads

13
BioCor
BioCor llrs R

Package to calculate functional similarity between genes https://biocor.llrs.dev

13
MicrobiomeR
MicrobiomeR vallenderlab R

A comprehensive R package for microbiome analysis.

13
libflagstats
libflagstats mklarqvist C

Efficient C functions to compute the summary statistics (flagstats) for sequencing read sets.

13
gene-oracle
gene-oracle SystemsGenetics Python

Feature extraction algorithm for genomic data

13