Author

Shyamal S. Mehtalia

Illumina (United States)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Approach:experimental assay· 1 Organism:human· 1 Approach:machine learning (classical)· 1

Frequent Co-Authors

Rami MehioiD· 2 shared Severine CatreuxiD· 2 shared Adam C. EnglishiD· 1 shared Arun VisvanathiD· 1 shared Breanna LeeiD· 1 shared C. KachulisiD· 1 shared Cooper RoddeyiD· 1 shared Daniel CameroniD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Rami MehioORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintApr 29, 2025

Celeste: A cloud-based genomics infrastructure with variant-calling pipeline suited for population-scale sequencing projects

Noora Siddiqui, Breanna Lee, Victoria Yi…·Eric Venner

Celeste provides a scalable cloud infrastructure for population-scale sequencing projects, including a variant-calling pipeline optimized for clinical variant detection.

DOI 10.1101/2025.04.29.25326690

humanwhole-genome sequencing

𝕏 PostBluesky

GenomicsbioRxivPreprintJan 2, 2024

Comprehensive and accurate genome analysis at scale using DRAGEN accelerated algorithms

Sairam Behera, Severine Catreux, Massimiliano Rossi…·Fritz Joachim Sedlazeck

DRAGEN provides fast and accurate genome analysis across 3,202 genomes, outperforming existing methods in variant detection speed and accuracy for various types including SNV, indel, STR, SV, and CNV.

39 citations

whole-genome sequencingmachine learning (classical)

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