Alexi Runnels

7PUBLICATIONS
143CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Cell and nuclear divisionGene expression (incl. microarray and other genome-wide approaches)Speciation and extinction
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Publications (7)

|May 18, 2026
The New York Genome Center ALS Consortium resource integrates postmortem tissue transcriptomics and whole genome sequencing to empower biological discovery.

|Dec 25, 2025
Benchmarking of duplex sequencing approaches to reveal somatic mutation landscapes.

Yang Zhang, Vinayak V Viswanadham, Michail Andreopoulos

|Nov 24, 2025
A comprehensive view of somatic mosaicism by single-cell DNA analysis.

Lovelace J Luquette, Tim H H Coorens, Abhiram Natu

|Nov 24, 2025
Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read data.

Yoo-Jin Jiny Ha, Dominika Maziec, Julia Markowski

|Aug 20, 2025
Paired plus-minus sequencing is an ultra-high throughput and accurate method for dual strand sequencing of DNA molecules.

Alexandre Pellan Cheng, Itai Rusinek, Aaron Sossin

|Aug 11, 2018
Transcriptome analysis of adult Caenorhabditis elegans cells reveals tissue-specific gene and isoform expression.

Rachel Kaletsky, Victoria Yao, April Williams

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Frequent Collaborators

4 joint publications

Soren Germer

3 joint publications

William C Feng

3 joint publications

Harsha V Doddapaneni

3 joint publications

Lisa Anderson