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TPMCalculator quantifies mRNA abundance directly from the alignments by parsing BAM files
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The need to understand cell developmental processes has spawned a plethora of computational methods for discovering hierarchies from scRNAseq data. However, existing techniques are based on Euclidean geometry which is not an optimal choice for modeling complex cell trajectories with multiple branches. To overcome this fundamental representation issue we propose Poincaré maps, a method harnessing the power of hyperbolic geometry into the realm of single-cell data analysis.
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MISO: Mixture of Isoforms model for RNA-Seq isoform quantitation
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Python library for processing (tandem) mass spectrometry data and for computing spectral similarities.
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🌲 An easy-to-use and scalable toolkit for genomic alteration signature (a.k.a. mutational signature) analysis and visualization in R https://shixiangwang.github.io/sigminer/reference/index.html
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Population-scale genotyping using pangenome graphs
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IT江湖 3D Touch Demo
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[Go] interface-bench - a quick look at some of Go's subtleties regarding the use of interfaces.
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IOBR is an R package to perform comprehensive analysis of tumor microenvironment and signatures for immuno-oncology.
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Nanopore data assembler
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序列号生成器--《万亿级调用系统:微信序列号生成器架构设计及演变》开源实现
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HTSeq is a Python library to facilitate processing and analysis of data from high-throughput sequencing (HTS) experiments.
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Pan-genome wide association studies
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🌶️ An ecosystem in Python for working with the Biological Expression Language (BEL)
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Short Read Sequence Typing for Bacterial Pathogens
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ENCODE Uniform processing pipeline for ChIP-seq
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Development repository for the Bioconductor package 'mixOmics '
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Codebook from my GWAS cookbook
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Ontology for rustling
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Biopieces is a bioinformatic framework of tools easily used and easily created.
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NGS Language Bindings
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Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
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Revolutionizing DNA analysis and making it accessible to all through innovative AI-powered analysis and interpretive tools
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Qiita - A multi-omics databasing effort
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Post-analysis of immune repertoire sequencing data
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A software package for calculating, applying, evaluating and plotting the results of polygenic risk scores
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Informed prediction and analysis of bacterial metabolic pathways and genome-scale networks
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Bayesian genotyper for structural variants
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Canvas - Copy number variant (CNV) calling from DNA sequencing data
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Search files for extensions as well as text within.
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Import and summarize transcript-level estimates for gene-level analysis
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Ranger-Mish-ImageWoof-5by lessw2020
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Repo to build on / reproduce the record breaking Ranger-Mish-SelfAttention setup on FastAI ImageWoof dataset 5 epochs
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SCP provides a comprehensive set of tools for single cell data processing and downstream analysis.
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Tools for processing UMI RNA-tag data
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Bioinformatics library for .NET
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Visual self-service analytics platform for big omics data.
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A tool for estimating repeat sizes
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Building classifiers using cancer transcriptomes across 33 different cancer-types
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TransVar - multiway annotator for precision medicine
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BGI-data-analysisby ehec-outbreak-crowdsourced
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assemblies, annotations, further analysis on sequenced strains from the EHEC outbreak
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Instrumented Principal Components Analysis
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Virus Identification By iteRative ANnoTation
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ComBat-seqby zhangyuqing
Batch effect adjustment based on negative binomial regression for RNA sequencing count data
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115
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muscatby HelenaLC
Multi-sample multi-group scRNA-seq analysis tools
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115
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TPMCalculatorby ncbi
TPMCalculator quantifies mRNA abundance directly from the alignments by parsing BAM files
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PoincareMapsby facebookresearch
The need to understand cell developmental processes has spawned a plethora of computational methods for discovering hierarchies from scRNAseq data. However, existing techniques are based on Euclidean geometry which is not an optimal choice for modeling complex cell trajectories with multiple branches. To overcome this fundamental representation issue we propose Poincaré maps, a method harnessing the power of hyperbolic geometry into the realm of single-cell data analysis.
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MISOby yarden
MISO: Mixture of Isoforms model for RNA-Seq isoform quantitation
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115
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flotillaby YeoLab
Reproducible machine learning analysis of gene expression and alternative splicing data
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matchmsby matchms
Python library for processing (tandem) mass spectrometry data and for computing spectral similarities.
Python
114
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sigminerby ShixiangWang
🌲 An easy-to-use and scalable toolkit for genomic alteration signature (a.k.a. mutational signature) analysis and visualization in R https://shixiangwang.github.io/sigminer/reference/index.html
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114
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graphtyperby DecodeGenetics
Population-scale genotyping using pangenome graphs
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114
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quickmergeby mahulchak
A simple and fast metassembler and assembly gap filler designed for long molecule based assemblies.
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114
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c
cgrangesby lh3
A C/C++ library for fast interval overlap queries (with a "bedtools coverage" example)
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BRANCHby baoe
Boosting RNA-Seq assemblies with partial or related genomic sequences
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interface-benchby teh-cmc
[Go] interface-bench - a quick look at some of Go's subtleties regarding the use of interfaces.
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IOBRby IOBR
IOBR is an R package to perform comprehensive analysis of tumor microenvironment and signatures for immuno-oncology.
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114
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GENESPACEby jtlovell
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seqsvrby nebula-chat
序列号生成器--《万亿级调用系统:微信序列号生成器架构设计及演变》开源实现
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113
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htseqby simon-anders
HTSeq is a Python library to facilitate processing and analysis of data from high-throughput sequencing (HTS) experiments.
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Scoaryby AdmiralenOla
Pan-genome wide association studies
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pybelby pybel
🌶️ An ecosystem in Python for working with the Biological Expression Language (BEL)
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pVACtoolsby griffithlab
Python
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srst2by katholt
Short Read Sequence Typing for Bacterial Pathogens
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112
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chip-seq-pipelineby ENCODE-DCC
ENCODE Uniform processing pipeline for ChIP-seq
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112
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mixOmicsby mixOmicsTeam
Development repository for the Bioconductor package 'mixOmics '
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gwas_scriptsby JoniColeman
Codebook from my GWAS cookbook
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112
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rustling-ontologyby snipsco
Ontology for rustling
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biopiecesby maasha
Biopieces is a bioinformatic framework of tools easily used and easily created.
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n
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gubbinsby nickjcroucher
Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
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112
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DNAnalyzerby VerisimilitudeX
Revolutionizing DNA analysis and making it accessible to all through innovative AI-powered analysis and interpretive tools
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112
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qiitaby qiita-spots
Qiita - A multi-omics databasing effort
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111
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vdjtoolsby mikessh
Post-analysis of immune repertoire sequencing data
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111
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PRSiceby choishingwan
A software package for calculating, applying, evaluating and plotting the results of polygenic risk scores
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gapseqby jotech
Informed prediction and analysis of bacterial metabolic pathways and genome-scale networks
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111
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svtyperby hall-lab
Bayesian genotyper for structural variants
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110
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canvasby Illumina
Canvas - Copy number variant (CNV) calling from DNA sequencing data
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SharpSearchby djhohnstein
Search files for extensions as well as text within.
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110
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tximportby mikelove
Import and summarize transcript-level estimates for gene-level analysis
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110
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Ranger-Mish-ImageWoof-5by lessw2020
Repo to build on / reproduce the record breaking Ranger-Mish-SelfAttention setup on FastAI ImageWoof dataset 5 epochs
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SCPby zhanghao-njmu
SCP provides a comprehensive set of tools for single cell data processing and downstream analysis.
R
110
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umisby vals
Tools for processing UMI RNA-tag data
Python
109
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bioby dotnetbio
Bioinformatics library for .NET
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109
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omicsplaygroundby bigomics
Visual self-service analytics platform for big omics data.
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109
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ExpansionHunterby Illumina
A tool for estimating repeat sizes
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109
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pancancerby greenelab
Building classifiers using cancer transcriptomes across 33 different cancer-types
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transvarby zwdzwd
TransVar - multiway annotator for precision medicine
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108
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BGI-data-analysisby ehec-outbreak-crowdsourced
assemblies, annotations, further analysis on sequenced strains from the EHEC outbreak
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108
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ipcaby bkelly-lab
Instrumented Principal Components Analysis
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108
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VIBRANTby AnantharamanLab
Virus Identification By iteRative ANnoTation
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108
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