|
Microarray
Papers of Note (January 2008)
|
| Journal |
Title |
Authors |
| American
Journal of Medical Genetics. 2008 Jan 17;146A(3):368-375 [Epub ahead
of print] |
Characterization
of a cryptic 3.3 Mb deletion in a patient with a "balanced t(15;22) translocation"
using high density oligo array CGH and gene expression arrays. |
Li MM,
et al. |
Analytical
and Bioanalytical Chemistry. 2008 Jan 18; [Epub ahead
of print] |
Genotypic
resistance testing in HIV by arrayed primer extension. |
Schanne
M, et al. |
Analytical
and Bioanalytical Chemistry. 2008 Jan 29; [Epub ahead
of print] |
Home-built
integrated microarray system (IMAS). A three-laser confocal fluorescence
scanner coupled with a microarray printer. |
Tragoulias
SS, et al. |
| Annals
of Human Genetics. 2008 Jan 20; [Epub ahead of print] |
Segmental
copy-number variation observed in Japanese by array-CGH. |
Takahashi
N, et al. |
| Applied
Immunohistochemistry & Molecular Morphology. 2008 Jan 25; [Epub
ahead of print] |
Tissue
microarrays for routine diagnostic assessment of HER2 status in breast carcinoma.
|
Drev P,
et al. |
| Biostatistics.
2008 Jan;9(1):51-65. |
Integrating
quantitative information from ChIP-chip experiments into motif finding.
|
Shim H,
et al. |
| Current
Opinions in Biotechnology. 2008 Jan 8; [Epub ahead of print] |
Human
protein atlas and the use of microarray technologies. |
Hober S,
et al. |
European
Journal of Human Genetics. 2008 Jan 16; [Epub ahead
of print] |
To
what extent do scans of non-synonymous SNPs complement denser genome-wide
association studies? |
Evans DM,
et al. |
| Gene.
2008 Jan 15;407(1-2):139-47. |
Genome-wide
combination profiling of copy number and methylation offers an approach
for deciphering misregulation and development in cancer cells. |
Park JJ,
et al. |
| Genetics
in Medicine. 2008 Jan;10(1):13-8. |
Pre-
and postnatal genetic testing by array-comparative genomic hybridization:
genetic counseling perspectives. |
Darilek
S, et al. |
| Human
Mutations. 2008 Jan;29(1):190-7. |
Array-MLPA:
comprehensive detection of deletions and duplications and its application
to DMD patients. |
Zeng F,
et al. |
| Journal
of Biopharmaceutical Statistics. 2008;18(1):183-202. |
Challenges
in DNA microarray studies from the regulatory perspective. |
Lababidi
S |
| Journal
of Medical Genetics. 2008 Jan 4; [Epub ahead of print] |
Comparison
of targeted and whole genome analysis of postnatal specimens using a commercially
available aCGH microarray platform. |
Aston E,
et al. |
| Molecular
Biotechnology. 2008 Jan;38(1):19-31. |
Validation
and quality control of protein microarray-based analytical methods.
|
Kricka
LJ, et al. |
| New
England Journal of Medicine. 2008 Jan 9; [Epub ahead of print] |
Association
between microdeletion and microduplication at 16p11.2 and autism. |
Weiss LA,
et al. |
| Nucleic
Acids Research. 2008 Jan 24; [Epub ahead of print] |
Discriminating
single-base difference miRNA expressions using microarray Probe Design Guru
(ProDeG). |
Lee I,
et al. |
| Nucleic
Acids Research. 2008 Jan 4; [Epub ahead of print] |
Model-based
variance-stabilizing transformation for Illumina microarray data. |
Lin SM,
et al. |
| Nucleic
Acids Research. 2008 Jan;36(1):e7. |
In
situ oligonucleotide synthesis on carbon materials: stable substrates
for microarray fabrication. |
Phillips
MF, et al. |
| Pharmacogenomics.
2008 Jan;9(1):5-9. |
Ultra-high-throughput
sequencing, microarray-based genomic selection and pharmacogenomics.
|
Hardiman
G, et al. |