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Author Details
Full Name
Zechen Chong
Affiliation
Heersink School of Medicine, University of Alabama at Birmingham
ORCID
Career Start Year
2011
Papers
38
H Index
21
Expertise
CM4AI Collaborator
Jake Y. Chen (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36650186
Deciphering the exact breakpoints of structural variations using long sequencing reads with DeBreak.
Nat Commun
2023
36650186
Deciphering the exact breakpoints of structural variations using long sequencing reads with DeBreak.
Nat Commun
2023
36152748
Protein arginine methyltransferase 1 in the generation of immune megakaryocytes: A perspective review.
J Biol Chem
2022
36152748
Protein arginine methyltransferase 1 in the generation of immune megakaryocytes: A perspective review.
J Biol Chem
2022
36008408
Selective suppression of melanoma lacking IFN-γ pathway by JAK inhibition depends on T cells and host TNF signaling.
Nat Commun
2022
35994499
Reduced sister chromatid cohesion acts as a tumor penetrance modifier.
PLoS Genet
2022
35546658
B-assembler: a circular bacterial genome assembler.
BMC Genomics
2022
35546658
B-assembler: a circular bacterial genome assembler.
BMC Genomics
2022
35994499
Reduced sister chromatid cohesion acts as a tumor penetrance modifier.
PLoS Genet
2022
36008408
Selective suppression of melanoma lacking IFN-γ pathway by JAK inhibition depends on T cells and host TNF signaling.
Nat Commun
2022
31180898
Scalable De Novo Genome Assembly Using a Pregel-Like Graph-Parallel System.
IEEE/ACM Trans Comput Biol Bioinform
2021
33632895
Haplotype-resolved diverse human genomes and integrated analysis of structural variation.
Science
2021
33554118
ClipSV: improving structural variation detection by read extension, spliced alignment and tree-based decision rules.
NAR Genom Bioinform
2021
34775997
Accurate long-read de novo assembly evaluation with Inspector.
Genome Biol
2021
35121884
RNF2 ablation reprograms the tumor-immune microenvironment and stimulates durable NK and CD4<sup>+</sup> T-cell-dependent antitumor immunity.
Nat Cancer
2021
31180898
Scalable De Novo Genome Assembly Using a Pregel-Like Graph-Parallel System.
IEEE/ACM Trans Comput Biol Bioinform
2021
33554118
ClipSV: improving structural variation detection by read extension, spliced alignment and tree-based decision rules.
NAR Genom Bioinform
2021
33632895
Haplotype-resolved diverse human genomes and integrated analysis of structural variation.
Science
2021
35121884
RNF2 ablation reprograms the tumor-immune microenvironment and stimulates durable NK and CD4<sup>+</sup> T-cell-dependent antitumor immunity.
Nat Cancer
2021
34775997
Accurate long-read de novo assembly evaluation with Inspector.
Genome Biol
2021
32568209
Ozone and Particulate Matter Exposure and Alzheimer's Disease: A Review of Human and Animal Studies.
J Alzheimers Dis
2020
32568209
Ozone and Particulate Matter Exposure and Alzheimer's Disease: A Review of Human and Animal Studies.
J Alzheimers Dis
2020
30827684
Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2.
Cell
2019
30827684
Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2.
Cell
2019
29696747
Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes.
Hum Mutat
2018
30030418
Regenerative Potential of Neonatal Porcine Hearts.
Circulation
2018
30400818
Combining accurate tumor genome simulation with crowdsourcing to benchmark somatic structural variant detection.
Genome Biol
2018
30013058
In vivo screening identifies GATAD2B as a metastasis driver in KRAS-driven lung cancer.
Nat Commun
2018
30039369
Structural Variant Breakpoint Detection with novoBreak.
Methods Mol Biol
2018
29696747
Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes.
Hum Mutat
2018
30013058
In vivo screening identifies GATAD2B as a metastasis driver in KRAS-driven lung cancer.
Nat Commun
2018
30039369
Structural Variant Breakpoint Detection with novoBreak.
Methods Mol Biol
2018
30030418
Regenerative Potential of Neonatal Porcine Hearts.
Circulation
2018
30400818
Combining accurate tumor genome simulation with crowdsourcing to benchmark somatic structural variant detection.
Genome Biol
2018
27892959
novoBreak: local assembly for breakpoint detection in cancer genomes.
Nat Methods
2017
28439535
A murine preclinical syngeneic transplantation model for breast cancer precision medicine.
Sci Adv
2017
27892959
novoBreak: local assembly for breakpoint detection in cancer genomes.
Nat Methods
2017
28235197
An Organismal CNV Mutator Phenotype Restricted to Early Human Development.
Cell
2017
28439535
A murine preclinical syngeneic transplantation model for breast cancer precision medicine.
Sci Adv
2017
28235197
An Organismal CNV Mutator Phenotype Restricted to Early Human Development.
Cell
2017
26806015
Functional annotation of rare gene aberration drivers of pancreatic cancer.
Nat Commun
2016
26806015
Functional annotation of rare gene aberration drivers of pancreatic cancer.
Nat Commun
2016
27356755
Hotspot mutations delineating diverse mutational signatures and biological utilities across cancer types.
BMC Genomics
2016
27841430
Single-cell isolation by a modular single-cell pipette for RNA-sequencing.
Lab Chip
2016
27841430
Single-cell isolation by a modular single-cell pipette for RNA-sequencing.
Lab Chip
2016
27356755
Hotspot mutations delineating diverse mutational signatures and biological utilities across cancer types.
BMC Genomics
2016
25762640
Genome-wide 5-hydroxymethylcytosine modification pattern is a novel epigenetic feature of globozoospermia.
Oncotarget
2015
25918555
ClinSeK: a targeted variant characterization framework for clinical sequencing.
Genome Med
2015
25626406
Clinical actionability enhanced through deep targeted sequencing of solid tumors.
Clin Chem
2015
25762640
Genome-wide 5-hydroxymethylcytosine modification pattern is a novel epigenetic feature of globozoospermia.
Oncotarget
2015
1 - 50 of 76
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Baylor College of Medicine
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University of California los angeles
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University of Texas MD Anderson Cancer Center
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European Bioinformatics Institute (EMBL-EBI)
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University of Heidelberg
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