An exploration of machine-learning based variant callers for SNV and small-indel using PacBio HiFi data

Benchmarking state-of-the-art secondary variant calling pipelines

Perform genome-wide association analysis to identify exome variants in Alzheimer's disease in UK

Towards a Truly “Personalized” Genome Part 2:

De novo assembly and haplotype phasing of diploid human…

How to Perform Large-scale Data Processing in Bioinformatics

GWAS Fine-Mapping Case Study: The Effects of Genomic Annotations on Resolution

Peter Nguyen, DNAnexus…

Towards a Truly “Personalized” Genome:

Part 1: De novo assembly and haplotype phasing diploid of human…

Single-cell sequencing on DNAnexus: Smart-Seq2 pipeline

Are you susceptible to adverse drug reactions?

Prediction and insights using LightGBM and SHAP — Part…

Trending topics in Bioinformatics & AI: the Magic of HLAs on Organs, COVID-19, and Love