Shloka Negi

6PUBLICATIONS
104CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Geoscience data visualisationEpigenetics (incl. genome methylation and epigenomics)Cancer geneticsGene mapping
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Publications (6)

|Jul 03, 2026
Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencing.

|Nov 19, 2025
Rapid, accurate long- and short-read mapping to large pangenome graphs with vg Giraffe.

Xian Chang, Adam M Novak, Jordan M Eizenga

|Sep 26, 2025
A complete diploid human genome benchmark for personalized genomics.

Nancy F Hansen, Nathan Dwarshuis, Hyun Joo Ji

|Feb 24, 2025
Long-read sequencing resolves the clinically relevant CYP21A2 locus, supporting a new clinical test for Congenital Adrenal Hyperplasia.

Jean Monlong, Xiao Chen, Hayk Barseghyan

|Sep 04, 2024
Advancing long-read nanopore genome assembly and accurate variant calling for rare disease detection.

Shloka Negi, Sarah L Stenton, Seth I Berger

|Feb 12, 2022
Nanotherapeutics in autophagy: a paradigm shift in cancer treatment.

Shloka Negi, Aiswarya Chaudhuri, Dulla Naveen Kumar

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Frequent Collaborators

3 joint publications

Karen H Miga

3 joint publications

Jean Monlong

3 joint publications

Emmanuèle Délot

3 joint publications

Benedict Paten