High-resolution mapping of copy-number alterations with massively parallel sequencing. - Wikidata - awgldk - TriplyDB

High-resolution mapping of copy-number alterations with massively parallel sequencing.

High-resolution mapping of copy-number alterations with massively parallel sequencing.

http://www.wikidata.org/entity/Q37072451

about

GROM-RD: resolving genomic biases to improve read depth detection of copy number variants COPS: a sensitive and accurate tool for detecting somatic Copy Number Alterations using short-read sequence data from paired samples Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives Tumor transcriptome sequencing reveals allelic expression imbalances associated with copy number alterations Accurate and comprehensive sequencing of personal genomes DELLY: structural variant discovery by integrated paired-end and split-read analysis TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology Mapping copy number variation by population-scale genome sequencing Biases in Illumina transcriptome sequencing caused by random hexamer priming VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library Whole-genome cancer analysis as an approach to deeper understanding of tumour biology Overview of recurrent chromosomal losses in retinoblastoma detected by low coverage next generation sequencing Next-Generation Sequencing Approaches in Cancer: Where Have They Brought Us and Where Will They Take Us?Approaches to isolation and molecular characterization of disseminated tumor cells Visualizing genome and systems biology: technologies, tools, implementation techniques and trends, past, present and future Not All Next Generation Sequencing Diagnostics are Created Equal: Understanding the Nuances of Solid Tumor Assay Design for Somatic Mutation Detection Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challenges Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine.New insights into the generation and role of de novo mutations in health and disease Computational characterisation of cancer molecular profiles derived using next generation sequencing Detection of Genomic Structural Variants from Next-Generation Sequencing Data Development of personalized tumor biomarkers using massively parallel sequencing Analysis of next-generation genomic data in cancer: accomplishments and challenges CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing Detectable clonal mosaicism in the human genome Multiple mutations in heterogeneous miltefosine-resistant Leishmania major population as determined by whole genome sequencing Genetic aberrations in imatinib-resistant dermatofibrosarcoma protuberans revealed by whole genome sequencing Intrachromosomal amplification, locus deletion and point mutation in the aquaglyceroporin AQP1 gene in antimony resistant Leishmania (Viannia) guyanensis Different Mutations in a P-type ATPase Transporter in Leishmania Parasites are Associated with Cross-resistance to Two Leading Drugs by Distinct Mechanisms Tumour evolution inferred by single-cell sequencing The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation Summarizing and correcting the GC content bias in high-throughput sequencing Next-generation genomics: an integrative approach Prenatal detection of aneuploidy and imbalanced chromosomal arrangements by massively parallel sequencing Genome-wide profiling of structural genomic variations in Korean HapMap individuals Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics Gene Expression Variations in Microsatellite Stable and Unstable Colon Cancer Cells Evaluation of statistical methods for normalization and differential expression in mRNA-Seq experiments Genome-wide copy number analysis of single cells.

P2860

Q21128696-F636C90A-3B72-40E4-B546-D96CE3C4C6F0 Q21133928-62072A9D-573A-45F1-B428-896EDBD37E5C Q21284304-2763CCBB-3865-4553-9FEF-D5BC9307C666 Q21562666-B184BD79-16CC-4BC1-B220-17AEFC49D9FB Q24604867-9EB83B49-6A2B-4DC7-BA84-3DEEB5E266D7 Q24605418-8499D309-9590-4E28-B0DC-9F253AF78B0D Q24613521-08525EE9-625F-446A-9BBA-8CB92436819A Q24615307-10F7DB19-39AB-425C-8279-70C3B33CAAC4 Q24620975-9127B424-9F47-452D-8FD2-63961CFF0A48 Q24628978-A2D3AFA0-2FEF-43D6-9BF1-CEA94F28A04C Q24633716-F40AE1FB-CF1A-473D-8989-55E8C06E36ED Q24653972-1725D427-BFBD-4AB3-9044-9AFBDBDAE106 Q26765431-A0E1BFEA-3E34-444E-B5B6-2E622F290EA0 Q26781271-77806932-C72F-4474-ACC6-02E44BAF3754 Q26785829-A945928C-F969-4582-837C-5C62A0408351 Q26796849-E1A23CF7-711E-4492-BC57-8BF2E4835CE8 Q26801745-FA8CCA9A-CDAA-49BE-ACBF-76C7625A1265 Q26864808-D10E2BB2-68F5-4224-8B24-EF585DD6DD94 Q27853005-2439620C-0A6D-4C4B-AEAA-B5CF30013B44 Q28073446-3C502539-C87F-4052-B713-E6EA821815A2 Q28080523-4BEEF8D3-5CC1-4866-A95A-17A207C4B7C0 Q28082859-DDBACEDF-D7DF-4CEF-9E7C-4B768B0A5E9F Q28278819-B94346C7-FAD8-4ABE-929F-C5F4366E7842 Q28293359-AD992110-5332-4315-BCD2-CAD60D3675DF Q28305453-0C1C84EF-6F86-4A6E-B5E4-A5151D98AEAE Q28392522-54ED88E9-16CB-4E3D-B6EF-EA046505A9AB Q28480626-A303A4B3-5BCC-4DB0-9939-4416D983DD98 Q28534967-264A0B0D-C01A-4856-BBD0-5CCC9507F67E Q28543469-18015783-B95F-4FFB-92A6-BE367B00EE0A Q28554770-6E832AD2-EC4A-4F30-B350-DE570FCC55B1 Q28646966-836041EA-A019-4CF1-B950-3F26585C80B7 Q28685216-1AB20ACB-4DC3-4B15-B6D4-70EA4C855557 Q28728245-25ABB423-044F-49CD-93E1-122D06B5DEC1 Q28730711-3BE2B942-796C-4B81-A33B-A893FA468B22 Q28731652-0268B7E1-0AC3-4E0D-A184-2B23946F717E Q28750551-B56E1582-E341-44E5-9614-5757F0161D21 Q28752377-E2D7D4D7-6E67-41A1-94F1-9018BF4F29B7 Q29304665-A557BBB4-E649-4F0C-BE48-A781E325FF9A Q29614452-6AB010E0-E1FF-4C20-B715-0347AA02753F Q30372139-022FEFFB-0408-4471-AC56-D010891E02A6

P2860

High-resolution mapping of copy-number alterations with massively parallel sequencing.

http://www.wikidata.org/entity/Q37072451

description

2008 nî lūn-bûn

@nan

2008年の論文

@ja

2008年学术文章

@wuu

2008年学术文章

@zh-cn

2008年学术文章

@zh-hans

2008年学术文章

@zh-my

2008年学术文章

@zh-sg

2008年學術文章

@yue

2008年學術文章

@zh

2008年學術文章

@zh-hant

name

High-resolution mapping of copy-number alterations with massively parallel sequencing.

@en

High-resolution mapping of copy-number alterations with massively parallel sequencing.

@nl

type

label

High-resolution mapping of copy-number alterations with massively parallel sequencing.

@en

High-resolution mapping of copy-number alterations with massively parallel sequencing.

@nl

altLabel

High-resolution mapping of copy-number alterations with massively parallel sequencing

@en

prefLabel

High-resolution mapping of copy-number alterations with massively parallel sequencing.

@en

High-resolution mapping of copy-number alterations with massively parallel sequencing.

@nl

P1433

Q37072451-36A9B725-E13A-4C2B-AA40-C8FDB57FCE04

P1476

Q37072451-0746BC48-9463-4E3B-B7F5-BE1E853A4C9B

P2093

Q37072451-17CDEBE5-B97B-4B35-9BDE-35D3553BC7C2

Q37072451-A7EEFDB0-C686-4C34-A024-F71863B8F493

Q37072451-B53772EE-193E-4367-821B-68BC893AC66C

Q37072451-B7B1B3C7-3EE4-403C-956E-0F553362DB34

Q37072451-E5B1B7B2-2F64-437E-BABF-55DDD14F83EB

P2860

Q37072451-3CFFC9D6-D746-4613-9026-3AE8DB0E94EA

Q37072451-470C0493-A470-4C88-8D85-2C65C9D4BE5E

Q37072451-4D24B156-D069-4A39-B44B-1E2109BDF204

Q37072451-60738E01-CD42-48CF-B9D6-C001C7804B21

Q37072451-64B6DC68-B8D5-4F32-8D34-1675E33FC13A

Q37072451-6CCA72D3-B566-441A-BD6B-1FCEAF964752

Q37072451-7A4DC4E5-F783-4220-9B96-414E91C451A3

Q37072451-87844CD6-B771-4FE6-A88F-B30687DD3BDE

Q37072451-97FF4E2D-984C-4BC4-8A7A-B4ED34749A22

Q37072451-9AE999A9-DF51-4C58-970C-73970BC426F8

P2888

Q37072451-07A92525-A920-4FBC-8469-8D74489DD1C1

P304

Q37072451-AD061603-8405-4953-8EC1-5FF38F45E13F

P31

Q37072451-BB4F6C06-C4A3-4F0A-A65E-3024127F5E42

P356

Q37072451-ECB46BD9-B0E0-4464-98C7-3F7EDF2F2874

P407

Q37072451-8ACCAACD-A361-4C74-8B17-305AB60DB0BC

P433

Q37072451-758AA792-1866-4453-9230-86B8D4303ED4

P478

Q37072451-62F8EA70-B370-48F7-929C-3539657D9AEB

P50

Q37072451-0041C1C8-DABB-4624-87C3-EB2BB3D9FE8B

Q37072451-1593ADE9-82E4-4D0D-A34B-1382A1A5C5D1

Q37072451-544032AF-D7DB-4C3F-9A2D-DF6411100E82

Q37072451-BA4806CF-542B-456E-8FE3-F6B219920CF3

Q37072451-C210E008-D936-4D93-BAB9-F9C892B0828D

P577

Q37072451-7F6CD3B0-DD3C-49D5-827D-C408FB24E4A5

P5875

Q37072451-16330B50-1717-4430-87F6-5D1472886738

P698

Q37072451-D0B370CF-F776-4038-AFF6-D83B8E404A5C

P932

Q37072451-FC1E1CE3-6293-481B-BF87-AD78095A185E

P356

P1433

P1476

High-resolution mapping of copy-number alterations with massively parallel sequencing.

@en

P2093

Carsten Russ

http://www.w3.org/2001/XMLSchema#string

David B Jaffe

http://www.w3.org/2001/XMLSchema#string

Michael J T O'Kelly

http://www.w3.org/2001/XMLSchema#string

Scott L Carter

http://www.w3.org/2001/XMLSchema#string

Xiaojun Zhao

http://www.w3.org/2001/XMLSchema#string

P2860

Digital karyotyping

Mapping and sequencing of structural variation from eight human genomes

Feedback circuit among INK4 tumor suppressors constrains human glioblastoma development

Amplification of a chromatin remodeling gene, Rsf-1/HBXAP, in ovarian carcinoma

Genome-wide maps of chromatin state in pluripotent and lineage-committed cells

Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

Paired-end mapping reveals extensive structural variation in the human genome

Comprehensive genomic characterization defines human glioblastoma genes and core pathways

Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution

Copy-number variation and association studies of human disease

P2888

P304

99-103

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1038/NMETH.1276

http://www.w3.org/2001/XMLSchema#string

P407

P433

1

http://www.w3.org/2001/XMLSchema#string

P478

6

http://www.w3.org/2001/XMLSchema#string

P50

Matthew Meyerson

P577

2008-11-30T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

23556373

http://www.w3.org/2001/XMLSchema#string

P698

19043412

http://www.w3.org/2001/XMLSchema#string

P932

2630795

http://www.w3.org/2001/XMLSchema#string