Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances.
about
pRb inactivation in mammary cells reveals common mechanisms for tumor initiation and progression in divergent epitheliaDigital karyotypingHigh-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridizationAutomated array-based genomic profiling in chronic lymphocytic leukemia: development of a clinical tool and discovery of recurrent genomic alterationsWhole-genome scanning by array comparative genomic hybridization as a clinical tool for risk assessment in chronic lymphocytic leukemiaArray comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndromeApplication of array-based comparative genomic hybridization to clinical diagnosticsMethods for high throughput validation of amplified fragment pools of BAC DNA for constructing high resolution CGH arraysA statistical approach for array CGH data analysisCombined subtractive cDNA cloning and array CGH: an efficient approach for identification of overexpressed genes in DNA ampliconsThe diagnosis and management of pre-invasive breast disease: promise of new technologies in understanding pre-invasive breast lesionsSW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization dataCGHPRO -- a comprehensive data analysis tool for array CGH.Progress in the application of DNA microarraysMicroarray comparative genomic hybridization detection of chromosomal imbalances in uterine cervix carcinoma.arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays.BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH)Different Facets of Copy Number Changes: Permanent, Transient, and AdaptivePatterns of Chromosomal Aberrations in Solid TumorsThe consequences of chromosomal aneuploidy on the transcriptome of cancer cellsHuman molecular cytogenetics: From cells to nucleotidesCopy number variations and strokeGenomic-Wide Analysis with Microarrays in Human OncologyArray-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalitiesCharacterization of human chromosomal material exchange with regard to the chromosome translocations using next-generation sequencing dataIntegrated DNA Copy Number and Gene Expression Regulatory Network Analysis of Non-small Cell Lung Cancer MetastasisAnalysis of molecular cytogenetic alteration in rhabdomyosarcoma by array comparative genomic hybridizationCNV-seq, a new method to detect copy number variation using high-throughput sequencingParsimonious higher-order hidden Markov models for improved array-CGH analysis with applications to Arabidopsis thaliana.Clinical implication of recurrent copy number alterations in hepatocellular carcinoma and putative oncogenes in recurrent gains on 1q.Integrated analysis of DNA copy number and gene expression microarray data using gene setsSpecific genomic regions are differentially affected by copy number alterations across distinct cancer types, in aggregated cytogenetic data.Bayesian mixture models for assessment of gene differential behaviour and prediction of pCR through the integration of copy number and gene expression data.Degenerate oligonucleotide primed-polymerase chain reaction-based array comparative genomic hybridization for extensive amplicon profiling of breast cancers : a new approach for the molecular analysis of paraffin-embedded cancer tissue.Progenetix: 12 years of oncogenomic data curation.The development of a mini-array for estimating the disease state of gastric adenocarcinoma by array CGHAn experimental loop design for the detection of constitutional chromosomal aberrations by array CGH.Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data.Exploiting noise in array CGH data to improve detection of DNA copy number change.
P2860
Q21090243-DCB9540A-DEFA-4309-9208-B2B866EEECD4Q22066241-5BFE236E-014B-4C18-8FE3-8546891CC1ABQ24530660-A870E2CF-09B2-4DBD-A516-8F941A8DF350Q24598248-A25D393A-DF92-43A8-B0A8-B4DE6197C344Q24642439-2C27AFEA-AF53-44E3-BFF0-0D5AEA737E91Q24674814-F0721AB4-612C-4DBE-87FB-498D54537D79Q24680375-CAEB0F86-F48C-4866-9EB1-3EC0D4E96D2EQ24681967-A3585EF4-6F3F-4636-BB00-375A9CE132C5Q24791257-6B7A269F-8278-4A8F-BEE4-2781BC13DA94Q24793620-59FE15C0-BE54-412F-AC05-0CA45D706370Q24799947-7F8BF2BE-0E7F-41A8-96FF-8ED1B3A8C88EQ24803014-115B341B-DD76-4232-A927-B97B0B157EFFQ24810415-B780D263-7CA9-4E1B-829F-8C8F5557C31DQ24811619-6ED87E4C-F23A-479D-A341-970F5E520E7FQ24813217-7F15217B-E118-4ADB-A918-B2B1C680F37BQ24813298-5E0E650B-B6DA-4C25-AF31-EF8651499245Q24815397-94A7BEF4-83F4-426F-B061-58A112935F65Q25257750-24E4E1A7-C0F5-419A-8E10-C6DC3E316297Q26769649-211EA995-56B0-4AE7-B0F1-4257D5D8E63DQ26786127-764BB4ED-588F-4674-BEB1-DB30F39AA8EAQ26995532-2A09444E-FA8E-400D-A490-81DB9AD55E3AQ27024633-7913F91B-DD01-437B-BCC5-BF6B1E80F9DFQ28067980-C5A4E107-075B-4F33-B674-678297D7A8B7Q28081059-E9F85E3B-72EF-4CA7-A59D-EF5F289AD761Q28296227-650C639B-4B32-4732-A7E4-CC98853FE11AQ28383593-F8A12884-1916-44BA-AA6D-7AB945CC2CCFQ28397049-9E03C991-A94B-4AB0-A0C0-7B73B91D8EBDQ28537996-AB7428F2-8529-4A98-B02F-E74B61436ADBQ29038143-B730C8AB-6351-4846-ADCD-F96F46E7B4FFQ30471421-C1311910-5481-4E2B-8341-74DAFFF69EF5Q30488297-CD3249BF-0216-473A-A41A-5E8871C48916Q30490621-44FFEE23-BC72-4477-8EEB-E830D0F33920Q30560230-4E25DAB4-A9ED-46FF-95AB-DB3E6CC159B5Q30656573-80C6CC85-BF79-4871-B7F6-7EA7ECD97571Q30666763-093AC735-A020-4FAB-AE8B-CF1F9227827CQ30694445-79BE75FB-2CEE-4B77-BBCA-6CEA153AAD91Q30856639-1C47FE59-02EB-48A6-8C8A-A8F05B53E669Q30898664-F4560EA9-84FA-4EE3-BF53-5AFD81B0AA18Q30998407-A187DB42-90AA-4D1B-8501-ABCF631CB590Q31097345-FD38673E-CEAC-42CA-B5D1-8AE235540147
P2860
Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances.
description
1997 nî lūn-bûn
@nan
1997 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Matrix-based comparative genom ...... screen for genomic imbalances.
@ast
Matrix-based comparative genom ...... screen for genomic imbalances.
@en
type
label
Matrix-based comparative genom ...... screen for genomic imbalances.
@ast
Matrix-based comparative genom ...... screen for genomic imbalances.
@en
prefLabel
Matrix-based comparative genom ...... screen for genomic imbalances.
@ast
Matrix-based comparative genom ...... screen for genomic imbalances.
@en
P2093
P1476
Matrix-based comparative genom ...... screen for genomic imbalances.
@en
P2093
Nickolenko J
Solinas-Toldo S
Stilgenbauer S
P304
P356
10.1002/(SICI)1098-2264(199712)20:4<399::AID-GCC12>3.3.CO;2-L
P577
1997-12-01T00:00:00Z