SPANDx workflow for analysis of haploid next-generation re-sequencing data.
Number of SNVs called by GATK-UGT with different cutoffs of genotype
SPANDx workflow for analysis of haploid next-generation re-sequencing data.
Investigation of Respiratory Syncytial Virus Outbreak on an Adult Stem Cell Transplant Unit by Use of Whole-Genome Sequencing
Spermatid-Specific Expression of the Novel X-Linked Gene Product SPAN-X Localized to the Nucleus of Human Spermatozoa1
Journal of Cellular Physiology, Cell Biology Journal
PDF) SPANDx: A genomics pipeline for comparative analysis of large haploid whole genome re-sequencing datasets
My Biosoftware – Bioinformatics Softwares Blog – Page 894 – Supply Bioinformatics Softwares Everyday
NGSgo-MX6-1
SPANDx workflow for analysis of haploid next-generation re-sequencing data.
