NGS catalog: A database of next generation sequencing studies in humans. - Wikidata - wikimedia - TriplyDB

NGS catalog: A database of next generation sequencing studies in humans.

NGS catalog: A database of next generation sequencing studies in humans.

http://www.wikidata.org/entity/Q35607189

about

Molecular Pathology and Personalized Medicine: The Dawn of a New Era in Companion Diagnostics-Practical Considerations about Companion Diagnostics for Non-Small-Cell-Lung-Cancer Predictive biomarkers for treatment selection: statistical considerations Personalized pathway enrichment map of putative cancer genes from next generation sequencing data In-depth comparison of somatic point mutation callers based on different tumor next-generation sequencing depth data Identification of phenylpropanoid biosynthetic genes and phenylpropanoid accumulation by transcriptome analysis of Lycium chinense A meta-analysis of somatic mutations from next generation sequencing of 241 melanomas: a road map for the study of genes with potential clinical relevance.Consensus rules in variant detection from next-generation sequencing data Characterization of early transcriptional responses to cadmium in the root and leaf of Cd-resistant Salix matsudana Koidz.Transcriptome and metabolome analysis in shoot and root of Valeriana fauriei.PAGER: constructing PAGs and new PAG-PAG relationships for network biology.Huvariome: a web server resource of whole genome next-generation sequencing allelic frequencies to aid in pathological candidate gene selection.Application of next generation sequencing to human gene fusion detection: computational tools, features and perspectives Deep sequencing and in silico analyses identify MYB-regulated gene networks and signaling pathways in pancreatic cancer.Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay.Genetic variations and alternative splicing: the Glioma associated oncogene 1, GLI1.Making headway with genetic diagnostics of intellectual disabilities.Cancer genomics and inherited risk.Methods: for studying pharmacogenetic profiles of combination chemotherapeutic drugs.CNVannotator: a comprehensive annotation server for copy number variation in the human genome.High Throughput Sequencing for Detection of Foodborne Pathogens.PAGER 2.0: an update to the pathway, annotated-list and gene-signature electronic repository for Human Network Biology.

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P2860

NGS catalog: A database of next generation sequencing studies in humans.

http://www.wikidata.org/entity/Q35607189

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2012 nî lūn-bûn

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NGS catalog: A database of next generation sequencing studies in humans.

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NGS catalog: A database of next generation sequencing studies in humans.

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NGS catalog: A database of next generation sequencing studies in humans.

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NGS catalog: A database of next generation sequencing studies in humans.

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NGS catalog: A database of next generation sequencing studies in humans.

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Bing Wang

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Junfeng Xia

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Peilin Jia

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Qingguo Wang

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Zhongming Zhao

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P2860

Deep RNA sequencing analysis of readthrough gene fusions in human prostate adenocarcinoma and reference samples

U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line

The diploid genome sequence of an Asian individual

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

Complete Khoisan and Bantu genomes from southern Africa.

The complete genome of an individual by massively parallel DNA sequencing

Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss

Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis

A small-cell lung cancer genome with complex signatures of tobacco exposure

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10.1002/HUMU.22096

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