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Top 20 rna-seq Open-Source Projects
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rnaseq
RNA sequencing analysis pipeline using STAR, RSEM, HISAT2 or Salmon with gene/isoform counts and extensive quality control.
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InfluxDB
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salmon
🐟 🍣 🍱 Highly-accurate & wicked fast transcript-level quantification from RNA-seq reads using selective alignment (by COMBINE-lab)
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mixcr
MiXCR is an ultimate software platform for analysis of Next-Generation Sequencing (NGS) data for immune profiling.
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alevin-fry
🐟 🔬🦀 alevin-fry is an efficient and flexible tool for processing single-cell sequencing data, currently focused on single-cell transcriptomics and feature barcoding.
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SaaSHub
SaaSHub - Software Alternatives and Reviews. SaaSHub helps you find the best software and product alternatives
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TPMCalculator
TPMCalculator quantifies mRNA abundance directly from the alignments by parsing BAM files
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COVID-19-RNA-Seq-datasets
A repository for sharing information on available COVID-19 RNA-Seq datasets
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rna-seq-kallisto-sleuth
A Snakemake workflow for differential expression analysis of RNA-seq data with Kallisto and Sleuth.
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popscle
A suite of population scale analysis tools for single-cell genomics data including implementation of Demuxlet / Freemuxlet methods and auxilary tools
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seq-pipeline
Workspace for data science projects and NGS pipelines. Contains RStudio, Jupyter Notebook, VSCode and file manager. Can connect to Tailscale network to bypass firewalls.
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gEAR
The gEAR Portal was created as a data archive and viewer for gene expression data including microarrays, bulk RNA-Seq, single-cell RNA-Seq and more. (by IGS)
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SaaSHub
SaaSHub - Software Alternatives and Reviews. SaaSHub helps you find the best software and product alternatives
https://github.com/owkin/PyDESeq2/blob/main/pydeseq2/preprocessing.py I'm not sure but only a normalized count matrix seems not enough to do differential expression analysis. For example, in this script, it gathers also the size factor from the raw read count matrix. Maybe you could find it somewhere or recalculate it.
Project mention: How can I read single cell data into scanpy? txt files | /r/bioinformatics | 2023-06-23
rna-seq related posts
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DESeq2 Normalization
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Point of using Hisat2 build to index reference genomes when working with known genomes mouse/human?
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I used featureCounts to quantify RNA-seq reads and got a low successful alignment percentage. Is this a problem?
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Any links to R-scripts for common NGS pipelines?
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How to create VCFs for scRNA-Seq data sets
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How to know where to align if I have RNAseq data??
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Pipeline to analyze ATAC seq
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A note from our sponsor - InfluxDB
www.influxdata.com | 3 May 2024
Index
What are some of the best open-source rna-seq projects? This list will help you:
Project | Stars | |
---|---|---|
1 | RNA-seq-analysis | 809 |
2 | rnaseq | 780 |
3 | salmon | 728 |
4 | PyDESeq2 | 516 |
5 | mixcr | 310 |
6 | bambu | 163 |
7 | alevin-fry | 149 |
8 | rnaseqc | 140 |
9 | TPMCalculator | 122 |
10 | clustifyr | 101 |
11 | COVID-19-RNA-Seq-datasets | 75 |
12 | cellSNP | 69 |
13 | diffexpr | 68 |
14 | rna-seq-kallisto-sleuth | 63 |
15 | popscle | 43 |
16 | wiggleplotr | 33 |
17 | zarp | 29 |
18 | seq-pipeline | 10 |
19 | gEAR | 10 |
20 | rnaseq | 6 |
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