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A robust benchmark for detection of germline large deletions and insertions

artículo científico publicado en 2020

Author Correction: A robust benchmark for detection of germline large deletions and insertions

artículo científico publicado en 2020

Background Mutations in Parental Cells Account for Most of the Genetic Heterogeneity of Induced Pluripotent Stem Cells ⬇️

artículo científico publicado el 26 de abril de 2012

Bi-order multimodal integration of single-cell data

artículo científico publicado en 2022

Clinical and Molecular Characterization of <i>POLE</i> Mutations as Predictive Biomarkers of Response to Immune Checkpoint Inhibitors in Advanced Cancers

scientific article published in 2022

Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing ⬇️

artículo científico publicado el 11 de enero de 2012

Comprehensive Characterization of Cancer Driver Genes and Mutations

artículo científico publicado en 2018

Delineating copy number and clonal substructure in human tumors from single-cell transcriptomes

artículo científico publicado en 2021

Distinct biological types of ocular adnexal sebaceous carcinoma: HPV-driven and virus-negative tumors arise through non-overlapping molecular-genetic alterations

scientific article published on 12 November 2018

Driver Fusions and Their Implications in the Development and Treatment of Human Cancers

artículo científico publicado en 2018

Genetic Biomarkers Of Sensitivity and Resistance to Venetoclax Monotherapy in Patients With Relapsed Acute Myeloid Leukemia

scientific article published on 17 May 2018

Hybrid oncocytic/chromophobe renal tumors are molecularly distinct from oncocytoma and chromophobe renal cell carcinoma

scientific article published on 23 June 2019

Hypervirulent group A Streptococcus emergence in an acaspular background is associated with marked remodeling of the bacterial cell surface

artículo científico publicado en 2018

Integrated transcriptomic-genomic tool Texomer profiles cancer tissues

scientific article published on 15 April 2019

Latent periodic process inference from single-cell RNA-seq data

scientific article published on 18 March 2020

Massively Parallel Sequencing Approaches for Characterization of Structural Variation ⬇️

artículo científico publicado el 1 de enero de 2012

Multi-platform discovery of haplotype-resolved structural variation in human genomes

artículo científico publicado en 2019

Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition

artículo científico publicado en 2020

Prospective Clinical Sequencing of Adult Glioma

scientific article published on 29 March 2019

Relative Abundance of SARS-CoV-2 Entry Genes in the Enterocytes of the Lower Gastrointestinal Tract

artículo científico publicado en 2020

SCMarker: Ab initio marker selection for single cell transcriptome profiling

scientific article published on 28 October 2019

Single-cell dissection of intratumoral heterogeneity and lineage diversity in metastatic gastric adenocarcinoma

artículo científico publicado en 2021

Single-nuclei RNA-seq on human retinal tissue provides improved transcriptome profiling

scientific article published on 17 December 2019

SomaticSniper: identification of somatic point mutations in whole genome sequencing data ⬇️

artículo científico publicado el 6 de diciembre de 2011

Spatially interacting phosphorylation sites and mutations in cancer

artículo científico publicado en 2021

The Immune Landscape of Cancer

scientific article published on 01 August 2019

The Origin and Evolution of Mutations in Acute Myeloid Leukemia ⬇️

artículo científico publicado el 20 de julio de 2012

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