wegene-llc / weapp-developer-guide
WeGene 微解读专业版开发者文档
☆27Updated last year
Related projects ⓘ
Alternatives and complementary repositories for weapp-developer-guide
- wgs_pipeline☆18Updated 10 years ago
- ☆16Updated 7 years ago
- ☆88Updated 4 years ago
- CWL tools and workflows for GGR☆21Updated 3 years ago
- Command line tools for CMDB varaints browser☆23Updated 5 months ago
- parallel-fastq-dump implementation in bash script☆40Updated 4 years ago
- 软件方面的包 (包括各种芯片数据处理,NGS数据处理,差异分析等等!)☆14Updated 8 years ago
- BIC@MSKCC Variants Pipeline☆23Updated last year
- Documenting usage and experience with bioinformatic tools☆40Updated 9 years ago
- Samtools' manual in Chinese - Samtools中文使用手册☆17Updated 8 years ago
- Tools for next-generation sequencing analysis☆88Updated 5 years ago
- ☆67Updated 2 years ago
- Let's get started!☆15Updated 5 years ago
- openbiox 翻译计划☆16Updated 5 years ago
- identifying mutational significance in cancer genomes☆60Updated last year
- Do not use - please refer to our newest code: https://github.com/cgat-developers/cgat-apps☆124Updated 6 years ago
- New version☆33Updated 7 years ago
- Draw Circos in Python☆30Updated 2 years ago
- Estimate damage in standard NGS library preparation. Incompatible with library preparation methods from which the imbalance is lost (such…☆51Updated 7 years ago
- This repo has been archived, these workflows are still available in the GATK repository under the scripts directory. The workflows are al…☆76Updated 4 years ago
- Framework to process and call somatic variation from NGS dataset generated using MSK-IMPACT assay☆55Updated 3 years ago
- Calculate the Delta_Ct, Delta_Delta_Ct , Fold Changes and Student's t-tests from qRT-PCR experiment☆26Updated 4 years ago
- CADD scripts release for offline scoring. For more information about CADD, please visit our website☆72Updated this week
- A BioWDL pipeline for processing RNA-seq data, starting with FASTQ files to produce expression measures and VCFs. Category:Multi-Sample☆31Updated last year
- Python for HLA analysis: summary, association analysis, zygosity test and interaction test☆32Updated 3 months ago
- Introduction to Programming for Bioinformatics, based on previous GNBF5010 Introduction to Programming course in Chinese University of Ho…☆26Updated last year
- A tool to call somatic single nucleotide variants.☆40Updated 9 years ago
- De novo transcriptome assembler for short reads☆62Updated 6 years ago
- This script use to analyze the immune repertoire sequenced by high throughtput sequencing☆24Updated 2 years ago