Author details

Full Name

Minita Shah

Affiliation

ORCID

Career Start Year

2012

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37704749	Evolution of structural rearrangements in prostate cancer intracranial metastases.	NPJ Precis Oncol	2023
37919447	Author Correction: Evolution of structural rearrangements in prostate cancer intracranial metastases.	NPJ Precis Oncol	2023
35484108	Somatic whole genome dynamics of precancer in Barrett's esophagus reveals features associated with disease progression.	Nat Commun	2022
33241313	Somatic variant analysis of linked-reads sequencing data with Lancet.	Bioinformatics	2021
33007263	Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs.	Cell	2020
32483360	Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring.	Nat Med	2020
32918070	Author Correction: PGBD5 promotes site-specific oncogenic mutations in human tumors.	Nat Genet	2020
31375115	Correction to: Sequencing and curation strategies for identifying candidate glioblastoma treatments.	BMC Med Genomics	2019
31836783	Deep whole-genome sequencing of 3 cancer cell lines on 2 sequencing platforms.	Sci Rep	2019
31023376	Sequencing and curation strategies for identifying candidate glioblastoma treatments.	BMC Med Genomics	2019
29392687	Whole Genome Sequencing-Based Discovery of Structural Variants in Glioblastoma.	Methods Mol Biol	2018
30552129	A recurrent novel <i>MGA-NUTM1</i> fusion identifies a new subtype of high-grade spindle cell sarcoma.	Cold Spring Harb Mol Case Stud	2018
30138725	Analytical Validation of Clinical Whole-Genome and Transcriptome Sequencing of Patient-Derived Tumors for Reporting Targetable Variants in Cancer.	J Mol Diagn	2018
29853643	Organoid Profiling Identifies Common Responders to Chemotherapy in Pancreatic Cancer.	Cancer Discov	2018
30271907	Genome-wide somatic variant calling using localized colored de Bruijn graphs.	Commun Biol	2018
28740869	Comparing sequencing assays and human-machine analyses in actionable genomics for glioblastoma.	Neurol Genet	2017
28504702	PGBD5 promotes site-specific oncogenic mutations in human tumors.	Nat Genet	2017
28951624	Erratum: PGBD5 promotes site-specific oncogenic mutations in human tumors.	Nat Genet	2017
23824211	Novel Conserved Genotypes Correspond to Antibiotic Resistance Phenotypes of E. coli Clinical Isolates.	PLoS ONE	2013
23775370	A comprehensive assay for CFTR mutational analysis using next-generation sequencing.	Clin Chem	2013
22135348	Low-pass genome-wide sequencing and variant inference using identity-by-descent in an isolated human population.	Genetics	2012
22723055	The possibility of de novo assembly of the genome and population genomics of the mangrove rivulus, Kryptolebias marmoratus.	Integr Comp Biol	2012
22426219	New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing.	Nat Commun	2012