Results 141 to 150 of about 74,278 (259)

SNP Array Karyotyping Allows for the Detection of Uniparental Disomy and Cryptic Chromosomal Abnormalities in MDS/MPD-U and MPD

, 2007
Lukasz P. Gondek, Andrew Dunbar, Hadrian Szpurka, Michael A. McDevitt, Jaroslaw P. Maciejewski   +4 more
openalex   +2 more sources

CalMaTe: a method and software to improve allele-specific copy number of SNP arrays for downstream segmentation [PDF]

, 2012
María Ortiz-Estévez, Ander Aramburu, Henrik Bengtsson, Pierre Neuvial, Ángel Rubio   +4 more
openalex   +1 more source

Identification of a distinct epigenetic subgroup with inferior PFS in intracranial mesenchymal tumors with FET::CREB fusion

Brain Pathology, EarlyView.
Six new cases of intracranial mesenchymal tumors with FET::CREB fusion, alongside 20 previously reported cases underwent DNA methylation profiling uncovered a novel epigenetic subgroup distinguished by inferior PFS and unique clinicopathological, molecular, and epigenetic hallmarks.
Yong Lin, Yun Ning, Yang Lan, Yu‐Juan Cao, Rui‐Jiao Zhao, Hai‐Nan Li, Song Duan, Wei‐Wei Fu, Hai‐Bo Wu, Feng Wu, Xiu‐Wu Bian, Tao Luo, Xiao‐Hong Yao   +12 more
wiley   +1 more source

Comparison between SNP array and imputed data to estimate population structure and ROH hotspots in horse breeds. [PDF]

BMC Genomics
Chessari G, Reich P, Criscione A, Falker-Gieske C, Mastrangelo S, Tumino S, Bordonaro S, Marletta D, Tetens J.   +8 more
europepmc   +1 more source

Retraction: Genome-wide association mapping for high temperature tolerance in wheat through 90k SNP array using physiological and yield traits. [PDF]

PLoS One, 2023
PLOS ONE Editors.
europepmc   +1 more source

Development of an integrated 200K SNP genotyping array and application for genetic mapping, genome assembly improvement and genome wide association studies in pear (Pyrus) [PDF]

, 2019
Xiaolong Li, Jugpreet Singh, Mengfan Qin, Siwei Li, Xun Zhang, Mingyue Zhang, Awais Khan, Shaoling Zhang, Jun Wu   +8 more
openalex   +1 more source

Immunohistochemistry as a tool for identifying EGFR amplification in CNS tumors

Brain Pathology, EarlyView.
EGFR gene amplification constitutes a diagnostic hallmark for glioblastoma, IDH‐wildtype (GB, IDH‐WT). Herein, we demonstrated that EGFR IHC is a highly specific and sensitive biomarker for identifying EGFR amplification and should be part of the neuropathologist's routine panel of antibodies.
Arnault Tauziède‐Espariat, Mary Bah, Farah Sassi, Noémie Pucelle, Charlotte Berthaud, Marion Mandoula, Zeina Dababou, Noah Carnes, Leïla Brissez, Lauren Hasty, Euphrasie Servant, Alice Métais, Pascale Varlet   +12 more
wiley   +1 more source

First development of a 100 K SNP array for small yellow croaker and its application in genomic selection for growth and disease resistance. [PDF]

BMC Genomics
Liu F, Wang R, Ye T, Zhu J, Guo D, Zhan W, Lou B.   +6 more
europepmc   +1 more source

Identification of genomic aberrations associated with disease transformation by means of high‐resolution SNP array analysis in patients with myeloproliferative neoplasm [PDF]

, 2011
Elisa Rumi, Ashot S. Harutyunyan, Chiara Elena, Daniela Pietra, Thorsten Klampfl, Klaudia Bagienski, Tiina Berg, Ilaria Carola Casetti, Cristiana Pascutto, Francesco Passamonti, Róbert Královics, Mario Cazzola   +11 more
openalex   +1 more source

SNP Array Screening and Long Range PCR-Based Targeted Next Generation Sequencing for Autosomal Recessive Disease with Consanguinity: Insight from a Case of Xeroderma Pigmentosum Group C. [PDF]

Genes (Basel), 2023
Nomura F, Shimizu A, Togi S, Ura H, Niida Y.   +4 more
europepmc   +1 more source