Generate the Panel of Normal files for TNseq and TNscope.
Atjaunināts pirms 3 gadiem
Generating a VAF file from one FASTQ file parallelly. And then parallelized read the set of VAF files by vaf_ncm.py.
Atjaunināts pirms 3 gadiem
Atjaunināts pirms 3 gadiem
Generate a VAF file from the FASTQ file. The purpose of this app is that sometimes we have to process hundreds of files. In this case, using YaqingLiu/NGSCheckMate_parallel is not an optimal choice.
Atjaunināts pirms 3 gadiem
Infer and visualize copy number from high-throughput DNA sequencing data.
Atjaunināts pirms 4 gadiem
The coverage of 2315 genes selected from the Network of Cancer Genes (NCG).
Atjaunināts pirms 4 gadiem
Atjaunināts pirms 4 gadiem
Atjaunināts pirms 4 gadiem
Atjaunināts pirms 4 gadiem
Calculate the MD5 of INPUT files in bulk.
Atjaunināts pirms 4 gadiem
Atjaunināts pirms 4 gadiem
Atjaunināts pirms 4 gadiem
Atjaunināts pirms 4 gadiem
Variant calling using Varscan somatic, processSomatic and somaticFilter based on BAM file.
Atjaunināts pirms 4 gadiem
Calculate the bed coverage of multiple BAM files before and after dedup
Atjaunināts pirms 4 gadiem