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Tristen Ross
Institution:
Foundation Medicine (United States)
Observed institutions:
Claritas Genomics (United States),
Foundation Medicine (United States)
OpenAlex ID:
A5050968158
Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis
2014
·
Henne Holstege
, Wayne Pfeiffer
, et al.
·
Genome Research
·
155
A Comprehensive Assay for CFTR Mutational Analysis Using Next-Generation Sequencing
2013
·
Ahmad N Abou Tayoun
, Christopher D Tunkey
, et al.
·
Clinical Chemistry
·
49
Comparative genomics of 274 Vibrio cholerae genomes reveals mobile functions structuring three niche dimensions
2014
·
Bas E Dutilh
, Cristiane C Thompson
, et al.
·
BMC Genomics
·
28
PDF
Recurrent heteroplasmy for the MT-ATP6 p.Ser148Asn (m.8969G>A) mutation in patients with syndromic congenital sideroblastic anemia of variable clinical severity
2018
·
Simon Berhe
, Matthew M. Heeney
, et al.
·
Haematologica
·
14
PDF
Orthogonal NGS for High Throughput Clinical Diagnostics
2016
·
Niru Chennagiri
, Eric J. White
, et al.
·
Scientific Reports
·
14
PDF
Chasing a moving target: Detection of mitochondrial heteroplasmy for clinical diagnostics
2017
·
Eric J. White
, Tristen Ross
, et al.
·
bioRxiv (Cold Spring Harbor Laboratory)
·
6
PDF
Breadth versus depth: whole transcriptome sequencing has reduced sensitivity for detection of clinically relevant fusions compared to RNA comprehensive genomic profiling
2024
·
Rachel B Keller-Evans
, Daniela Munafo
, et al.
·
The Oncologist
·
4
A Comprehensive Assay for CFTR Mutational Analysis Using Next‐Generation Sequencing
2013
·
Ahmad N. Abou Tayoun
, Christopher D. Tunkey
, et al.
·
The FASEB Journal
·
3
Abstract 3927: Analytical performance of a novel tissue-informed non-bespoke whole genome MRD detection assay.
2026
·
David Delfosse
, Alexander Fine
, et al.
·
Cancer Research
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Works count:
9
Citation count:
273
H-index:
6
I10-index:
5
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