Genomic microarrays in human genetic disease and cancer. - Wikidata - awgldk - TriplyDB

Genomic microarrays in human genetic disease and cancer.

Genomic microarrays in human genetic disease and cancer.

http://www.wikidata.org/entity/Q35198389

about

COPS: a sensitive and accurate tool for detecting somatic Copy Number Alterations using short-read sequence data from paired samples High-resolution genomic profiles of human lung cancer High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridization Allele quantification using molecular inversion probes (MIP).Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features A statistical approach for array CGH data analysis Genetic alteration and gene expression modulation during cancer progression GEPAS, an experiment-oriented pipeline for the analysis of microarray gene expression data Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics Human molecular cytogenetics: From cells to nucleotides Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases Flexible and accurate detection of genomic copy-number changes from aCGH.New challenges in gene expression data analysis and the extended GEPAS Detecting deletions in families affected by a dominant disease by use of marker data.Next station in microarray data analysis: GEPAS.TEAM: a tool for the integration of expression, and linkage and association maps.A multiplex PCR predictor for aCGH success of FFPE samples.Tiling array-CGH for the assessment of genomic similarities among synchronous unilateral and bilateral invasive breast cancer tumor pairs.High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics FACADE: a fast and sensitive algorithm for the segmentation and calling of high resolution array CGH data rSW-seq: algorithm for detection of copy number alterations in deep sequencing data.A de novo genome assembly algorithm for repeats and nonrepeats Efficient change point detection for genomic sequences of continuous measurements.Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome.A method for generating selective DNA probes for the analysis of C-negative regions in human chromosomes.Piecing together the problems in diagnosing low-level chromosomal mosaicism.The database of chromosome imbalance regions and genes resided in lung cancer from Asian and Caucasian identified by array-comparative genomic hybridization Whole genome scanning identifies genotypes associated with recurrence and metastasis in prostate tumors.Genomic loss of tumor suppressor miRNA-204 promotes cancer cell migration and invasion by activating AKT/mTOR/Rac1 signaling and actin reorganization Genetics and pathology of pancreatic cancer.Optimizing high dimensional gene expression studies for immune response following smallpox vaccination using Taqman® low density immune arrays Guidelines for molecular karyotyping in constitutional genetic diagnosis.Cell-based Models for Discovery of Pharmacogenomic Markers of Anticancer Agent Toxicity.Cancer gene discovery in mouse and man.Array-CGH and breast cancer.High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping.High-resolution array CGH profiling identifies Na/K transporting ATPase interacting 2 (NKAIN2) as a predisposing candidate gene in neuroblastoma

P2860

Q21133928-390DAACA-4B29-4B47-8B12-4002294607FB Q24530598-A2DD7AE4-946B-489B-877E-275650CBD9E6 Q24530660-6491E47F-1487-4C43-BA96-E187A9D6BE8A Q24537476-FC9B8E2F-0146-49BA-A470-033C1EC85EDB Q24675632-BAC8AC46-21EF-4538-93B2-43037BE1D63D Q24793620-C0D3D237-B54E-48AF-803D-871A50989EFA Q24798750-531BCC07-257F-46A1-8166-89B9F323E9C0 Q24813561-7737423F-A383-4F6A-81BB-E031BAAD956E Q27023696-AFDB89FC-1847-43EF-A6E8-1CE8AC8D9597 Q27024633-34C3D2B5-AB20-4774-A2EF-21672899D2DA Q28236948-0B4C319C-2B71-48D5-A1F3-A6EE3C4D5A96 Q30479616-F2F3C983-23EB-4E52-A15D-9C00EA1E8DBB Q30939961-B1F9AC78-5AEA-4EE6-9F2E-73BD078D8A98 Q31001485-5A10B4D3-87F9-4BE8-9007-73316511D034 Q31048894-E61B9181-69ED-4AC4-8851-76C6997C371B Q31053596-E801BFBA-9450-4D45-9DC2-231361444C3F Q33228753-72D2AC07-FCA6-462A-B377-9B4D6A5E80BA Q33350663-43886867-B45F-4D30-B13C-CD007C2EEF8C Q33480832-65F33A39-108E-4B11-AB2D-05D56589F336 Q33529487-5B402AF3-C6F1-4C4A-9B2B-0265E6C6C589 Q33605550-47E7BDBE-51D7-4936-A67B-64258F915C75 Q33662745-735BFDE5-21A4-43B4-B10C-BD0BF667FA26 Q33748392-74A02B72-9750-459C-B0DF-C57C078B2C5E Q33750957-2FEFD7E0-D9A6-4143-86F2-926EE61BBD80 Q33905292-2891C53D-C710-4AB1-B153-B0F7D61029C2 Q33910274-B5607280-CCAE-4A00-A111-D492F162E522 Q33942262-47287BCB-4B63-476A-B351-3A35770C8B85 Q33979278-37DE72FF-DE7F-46E9-86E1-8E460356F6C5 Q34073503-2FA7AA3C-C70F-4C43-9704-EE346E1F2C2B Q34301249-21464C1F-CAC0-40DF-A9FB-6E1159FC7543 Q34320113-E70909B3-A921-4AC0-B107-76EC4E5ED53B Q34533814-97C91327-AC5A-47AB-9D86-7618D59B8EA4 Q34589293-6E04C32C-3F34-411C-8529-FCE3112D25F9 Q34634341-5C4CDD01-0B0B-4CBC-ABBE-0E3A6DFCF454 Q34653075-798E1957-CB69-4EBE-B78F-A6C5F04F859C Q34789161-0F06F825-287F-4485-B36B-F631B70332D7 Q34962407-10DBF61E-FAEE-48FC-8A6B-E36ABD6F4FD6 Q35012854-A57DF265-9FB6-43EB-BAD7-982A55D7A099 Q35012994-C6DAA7C1-4932-4B0C-9436-7A2A11847675 Q35036462-D3556477-2FCF-4C47-9C6B-F887F4ED2A8A

P2860

Genomic microarrays in human genetic disease and cancer.

http://www.wikidata.org/entity/Q35198389

description

2003 nî lūn-bûn

@nan

2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2003年の論文

@ja

2003年論文

@yue

2003年論文

@zh-hant

2003年論文

@zh-hk

2003年論文

@zh-mo

2003年論文

@zh-tw

2003年论文

@wuu

name

Genomic microarrays in human genetic disease and cancer.

@ast

Genomic microarrays in human genetic disease and cancer.

@en

type

label

Genomic microarrays in human genetic disease and cancer.

@ast

Genomic microarrays in human genetic disease and cancer.

@en

prefLabel

Genomic microarrays in human genetic disease and cancer.

@ast

Genomic microarrays in human genetic disease and cancer.

@en

P1433

Q35198389-CB92EB10-5309-4A64-815B-1E090999B05A

P1476

Q35198389-A7E78864-3330-42C4-95F3-5453F86A5457

P2093

Q35198389-23A82B64-E521-472F-8FA2-F1FAEA872E4A

Q35198389-62AACD20-72B5-4846-9071-CE252C0BAC60

P2860

Q35198389-0086096D-95D5-47FD-89D7-5D2500E8AFE4

Q35198389-0441E99C-2B9E-495A-A0D3-9855A3FD869C

Q35198389-1161F175-CF49-4579-9FAD-4BE621F11973

Q35198389-1371E392-1F83-466A-AEE9-EF1FB06C11A4

Q35198389-17F34286-DA21-4868-A4FD-182EB146FB5B

Q35198389-192A0DF0-3161-4E18-8F7E-61C13DF4B69C

Q35198389-1CAB3AED-9886-4BD4-9905-55D815DAA2F8

Q35198389-1F82615E-0C02-40D5-85D3-ED663165EAFB

Q35198389-223BB89D-1D99-435C-998E-F11138AFBE72

Q35198389-22EE51CE-A211-4E48-8C13-A96339E973CC

P304

Q35198389-3E191BE9-CA95-40C4-8AD6-79CFD700A7F8

P31

Q35198389-A7555E91-8B6C-4A4C-82C3-7F09CEBD3B5F

P356

Q35198389-7A513DD9-FBD8-41FB-9763-BAD273BF33A1

P478

Q35198389-025787F7-F641-4A8F-AEEE-36558A6A3D48

P577

Q35198389-4AC2A844-7C47-41F8-B9BF-E0454DEB727A

P5875

Q35198389-D94A32E7-282F-4018-925E-353F11BAC0ED

P698

Q35198389-B5092E4A-09E3-4C3B-880F-0E643B7EBC92

P356

P1433

Human Molecular Genetics

P1476

Genomic microarrays in human genetic disease and cancer.

@en

P2093

Daniel Pinkel

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

Donna G Albertson

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

P2860

Comprehensive copy number and gene expression profiling of the 17q23 amplicon in human breast cancer

ACVR1B (ALK4, activin receptor type 1B) gene mutations in pancreatic carcinoma

Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence

Genomic binding sites of the yeast cell-cycle transcription factors SBF and MBF

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

Genome-wide analysis of DNA copy-number changes using cDNA microarrays

Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH

Structure of chromosomal duplicons and their role in mediating human genomic disorders.

Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements.

P304

R145-52

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

P31

scholarly article

P356

10.1093/HMG/DDG261

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

P478

12 Spec No 2

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

P577

2003-08-05T00:00:00Z

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

P5875

10617038

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

P698

12915456

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