antigenomics / repseq-annotation-tutorial
📝 [Tutorial] RepSeq data mining basics in R
☆10Updated 6 years ago
Alternatives and similar repositories for repseq-annotation-tutorial
Users that are interested in repseq-annotation-tutorial are comparing it to the libraries listed below
Sorting:
- Identification of differentially methylated genes in biomedical data☆15Updated 6 years ago
- epigenome analysis to rank transcription factors☆13Updated 5 years ago
- ☆12Updated last year
- Mean Alterations Using Discrete Expression☆14Updated last year
- Perturb-seq analysis package☆14Updated last year
- Summary statistics for repertoires☆17Updated 2 years ago
- Pipeline for Ribosome Profiling Data☆16Updated last year
- Bioinformatics for Benched Biologists☆22Updated 5 years ago
- ChIP-seq DC and QC Pipeline☆34Updated 4 years ago
- A toolset for handling sequencing data with unique molecular identifiers (UMIs)☆15Updated 6 years ago
- ☆15Updated 2 years ago
- Workflow for the Association of T-cell receptors from 3' single-cell RNA-seq (WAT3R)☆21Updated 2 years ago
- Explore the cancer relevance of your gene list☆51Updated 2 months ago
- V'DJer - B Cell Receptor Repertoire Reconstruction from short read mRNA-Seq data☆29Updated 2 years ago
- 🧭 Navigate single-cell RNA-seq datasets in your web browser.☆28Updated last year
- A python tool to do comparative analysis of mulitple single cell datasets.☆22Updated 5 years ago
- Allele-Specific Expression by Single-Cell RNA Sequencing☆28Updated 4 years ago
- processes GoT amplicon data and generates a table of metrics☆29Updated 2 years ago
- SCAN2 is a somatic SNV and indel genotyper for single cells amplified by Primary Template-Directed Amplification (PTA)☆12Updated last week
- Using k-mers to call HLA alleles in RNA sequencing data☆22Updated 6 years ago
- scover☆23Updated last year
- GENIE3 (GEne Network Inference with Ensemble of trees) R-package☆30Updated 3 years ago
- Differential ATAC-seq toolkit☆27Updated last year
- Identify cell barcodes from single-cell genomics sequencing experiments☆43Updated 3 years ago
- Repository for the Anczukow-Lab splicing pipeline☆15Updated 2 months ago
- An interactive learning resource for next-generation sequencing (NGS) techniques☆29Updated 6 years ago
- S3norm ver2 + IDEAS epigenetic state / master peak list☆12Updated last year
- This is the BWA workflow used in the PanCancer project used to allign all the BAM files.☆11Updated 2 years ago
- Combined mutation recurrence and functional impact to identify coding and non-coding cancer drivers☆15Updated 6 years ago
- ☆12Updated 4 years ago