Assessing the significance of conserved genomic aberrations using high resolution genomic microarrays.
about
DiNAMIC: a method to identify recurrent DNA copy number aberrations in tumorsMultisample aCGH data analysis via total variation and spectral regularization.Functional copy-number alterations in cancer.Exploratory analysis of the copy number alterations in glioblastoma multiforme.CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data.Identification of recurrent regions of Copy-Number Variants across multiple individuals.Wavelet-based identification of DNA focal genomic aberrations from single nucleotide polymorphism arrays.A fused lasso latent feature model for analyzing multi-sample aCGH dataO-miner: an integrative platform for automated analysis and mining of -omics data.TAGCNA: a method to identify significant consensus events of copy number alterations in cancer.Comparative analysis of methods for identifying recurrent copy number alterations in cancer.A global transcriptional analysis of Plasmodium falciparum malaria reveals a novel family of telomere-associated lncRNAs.GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers.Genome-wide scan identifies a copy number variable region at 3p21.1 that influences the TLR9 expression levels in IgA nephropathy patientsGenome-wide integrative analysis revealed a correlation between lengths of copy number segments and corresponding gene expression profile.Osteoprotegerin secreted by inflammatory and invasive breast cancer cells induces aneuploidy, cell proliferation and angiogenesis.Penalized weighted low-rank approximation for robust recovery of recurrent copy number variations.Whole genome scanning as a cytogenetic tool in hematologic malignancies.High-resolution mapping of copy-number alterations with massively parallel sequencing.Combining chromosomal arm status and significantly aberrant genomic locations reveals new cancer subtypesA computational procedure to identify significant overlap of differentially expressed and genomic imbalanced regions in cancer datasets.Detection of recurrent copy number alterations in the genome: taking among-subject heterogeneity seriously.Statistical model-based testing to evaluate the recurrence of genomic aberrations.Multiple samples aCGH analysis for rare CNVs detection.Piecewise-constant and low-rank approximation for identification of recurrent copy number variations.
P2860
Q30498218-22B4997A-3C53-4CF9-A067-CF240A8AA081Q30631788-E4EF3A99-A0D8-45AA-809C-F6B531903A9DQ33368629-D4C50552-BBF7-491D-BA15-08A983F2A618Q33396458-6E2A25DE-0EF4-43C7-BF32-52C34D0C21D7Q33520628-5DA7AD3B-ECAA-4C95-BDC9-C1D5FBD79F69Q33543970-00462C92-A60D-44AF-9EE5-9F8277E6BC68Q33898563-68520907-9132-4CE1-A4E2-A9D19F87C138Q33923176-9726520C-D7EF-4FB5-9E99-E74708A4C232Q34273190-8D7B6722-AAEE-43C9-9985-A4D6541EAF36Q34345632-86DBBBE9-8CC4-437E-91F4-BAF82DAB79A1Q34534035-115BE3D9-FB24-4D35-9792-B0C76DCE98BDQ35557707-570A7ACB-4CC1-4E54-A30E-095E8EC5F36EQ35557782-D2FA3978-C664-4545-A4D2-66E0C37DD981Q35722106-ABEFF897-1BCA-4B6C-973B-C7AF78C7F0F7Q35759844-87C4351C-68DD-4B51-857A-9CC5A56F2422Q35853271-D0790936-5069-4886-BCB0-AFEF1F9DDFB1Q35864949-381A960C-2B0B-4078-B79B-F4ACA56947ADQ36835203-3FE7B385-0ECC-4214-9974-FD285E8939BDQ37072451-C64FCA17-2B3C-4FBC-8D4E-EC7F253F2A19Q37148663-699AEF35-ABE2-4953-A441-365F5BC96E4CQ37318482-50EFFE47-0C80-41A1-93B0-29CE542C1D0CQ37384126-5C9E6B9C-54C2-4264-8922-8F22FEF2B914Q39332745-54D07F9F-EAAB-48CE-9275-E5F3889AB5FAQ43116785-7EE2D2CF-F05D-477B-909E-19868BA23BB8Q46796492-61B902BE-31FC-4665-BE34-377468F32DB1
P2860
Assessing the significance of conserved genomic aberrations using high resolution genomic microarrays.
description
2007 nî lūn-bûn
@nan
2007 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Assessing the significance of ...... esolution genomic microarrays.
@ast
Assessing the significance of ...... esolution genomic microarrays.
@en
Assessing the significance of ...... esolution genomic microarrays.
@nl
type
label
Assessing the significance of ...... esolution genomic microarrays.
@ast
Assessing the significance of ...... esolution genomic microarrays.
@en
Assessing the significance of ...... esolution genomic microarrays.
@nl
prefLabel
Assessing the significance of ...... esolution genomic microarrays.
@ast
Assessing the significance of ...... esolution genomic microarrays.
@en
Assessing the significance of ...... esolution genomic microarrays.
@nl
P2093
P2860
P1433
P1476
Assessing the significance of ...... esolution genomic microarrays.
@en
P2093
Carolyn Mies
Christian J Stoeckert
Don A Baldwin
Katarzyna Dudycz-Sulicz
Mitchell Guttman
Sharon J Diskin
P2860
P356
10.1371/JOURNAL.PGEN.0030143
P577
2007-08-01T00:00:00Z