Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants.

Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants.

Item
http://www.wikidata.org/entity/Q31105539
Linked read sequencing resolves complex genomic rearrangements in gastric cancer metastases.NGSCheckMate: software for validating sample identity in next-generation sequencing studies within and across data types.Epigenetic Memory Underlies Cell-Autonomous Heterogeneous Behavior of Hematopoietic Stem CellsPysim-sv: a package for simulating structural variation data with GC-biases.The mutational landscape of ocular marginal zone lymphoma identifies frequent alterations in TNFAIP3 followed by mutations in TBL1XR1 and CREBBP.Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network.SVmine improves structural variation detection by integrative mining of predictions from multiple algorithms.Chromosome-scale mega-haplotypes enable digital karyotyping of cancer aneuploidy.Bioinformatics for precision oncology.PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation.Image-based drug screen identifies HDAC inhibitors as novel Golgi disruptors synergizing with JQ1.The characteristics of ctDNA reveal the high complexity in matching the corresponding tumor tissues.Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes.iCopyDAV: Integrated platform for copy number variations-Detection, annotation and visualization.Whole-genome sequencing reveals genomic signatures associated with the inflammatory microenvironments in Chinese NSCLC patients.SwissMTB: establishing comprehensive molecular cancer diagnostics in Swiss clinics
P2860

Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants.

Item
http://www.wikidata.org/entity/Q31105539
description
2016 nî lūn-bûn
@nan
2016 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Copy number analysis of whole- ...... ancer susceptibility variants.
@ast
Copy number analysis of whole- ...... ancer susceptibility variants.
@en
type
label
Copy number analysis of whole- ...... ancer susceptibility variants.
@ast
Copy number analysis of whole- ...... ancer susceptibility variants.
@en
prefLabel
Copy number analysis of whole- ...... ancer susceptibility variants.
@ast
Copy number analysis of whole- ...... ancer susceptibility variants.
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P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P932
P356
P1433
P1476
Copy number analysis of whole- ...... ancer susceptibility variants.
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P932