CNCBI / Samtools-Manual-CNLinks
Samtools' manual in Chinese - Samtools中文使用手册
☆17Updated 9 years ago
Alternatives and similar repositories for Samtools-Manual-CN
Users that are interested in Samtools-Manual-CN are comparing it to the libraries listed below
Sorting:
- Bowtie2's manual in Chinese - Bowtie2中文使用手册☆12Updated 9 years ago
- 361 Division - Scientific Training, Education and Learning☆28Updated 4 years ago
- ☆89Updated 4 years ago
- Maximum likelihood demultiplexing☆47Updated 4 months ago
- A fast and robust pre-processing pipeline for bulk or single-cell whole-genome bisulfite sequencing (WGBS) data.☆35Updated 3 years ago
- KOBAS: a command line tool for identifying significant pathways from genomic data☆30Updated 15 years ago
- ☆17Updated 4 years ago
- Scripts involved in our workflow for detecting CNVs from WGS data using read depth-based methods☆46Updated 2 years ago
- Command-line utility to color objects of a KEGG pathway with arbitrary colors☆33Updated 9 years ago
- Documenting usage and experience with bioinformatic tools☆40Updated 9 years ago
- Demultiplexes a fastq.☆44Updated 4 years ago
- Run Picard on BAM files and collate 90 metrics into one file.☆41Updated 7 years ago
- Software for predicting library complexity and genome coverage in high-throughput sequencing.☆85Updated 8 months ago
- ☆50Updated 6 years ago
- ☆51Updated 5 years ago
- Digenome-toolkit ver2.☆16Updated 3 years ago
- Scripts to run copynumber variation calls on tumor and normal BAM files using Varscan2☆29Updated 7 years ago
- A collection of tools to deal with Bisulfite-seq/NOMe-seq (SNP/Methylation calling: BisSNP; HMM segmentation: DMNTools; Visualization/Clu…☆32Updated 3 years ago
- reproduce the functional enrichment analysis presented in GTEx paper using clusterProfiler/DOSE☆33Updated 3 years ago
- Scripts for next generation sequencing☆48Updated 5 years ago
- ☆38Updated 4 years ago
- ☆49Updated 4 years ago
- Quality of RNA-Seq Toolset☆53Updated 6 years ago
- BS-seq analysis pipeline☆41Updated 2 years ago
- Arabidopsis RNA_-seq downstream analysis shiny app☆30Updated 5 years ago
- My own tools code for NGS data analysis (Next Generation Sequencing)☆30Updated 5 years ago
- Repository of common bioinformatics scripts☆39Updated 3 years ago
- RPKM for RNASeq counts☆16Updated 4 years ago
- High-intensity sequencing reveals the sources of plasma circulating cell-free DNA variants☆22Updated 5 years ago
- Pipeline for identifying viral integration and fusion mRNA reads from NGS data. Manuscript is currently in preparation.☆28Updated 3 years ago