Whole Genome Sequencing 1 article

Whole Genome Sequencing examines sequencing and interpretation across essentially the complete genome rather than targeted panels or selected exons. Coverage includes variant calling, structural variation, germline and somatic analysis, coverage quality, population studies and clinical interpretation where whole-genome data are central. Long-read sequencing belongs in its own category when read technology is the primary issue; this section is defined by genome-wide scope rather than by a particular sequencing platform.

Bioinformatics Methods & Tools

October 6, 2026, 1:14 PM · 3 mins read

Loyola bioinformatics students present machine learning breakthroughs at Great Plains conference

Two students from Dr. Wheeler's Lab at Loyola shared new research on machine learning and deep learning in genomics at the Great Plains Bioinformatics conference in Omaha. Their work targets antimalarial resistance and skin cancer gene discovery.