Sort   by:  
 Page size 
UnknownDirect and Indirect Role of Migratory Birds in Spreading CCHFV and WNV: A Multidisciplinary Study on Three Stop-Over Islands in Italy.
Not available
S-EPMC9505975 | biostudies-literature
UnknownTick Species Diversity and Molecular Identification of Spotted Fever Group Rickettsiae Collected from Migratory Birds Arriving from Africa.
Not available
S-EPMC10458931 | biostudies-literature
Genomicsena-DATASET-UHN-12-07-2016-18:07:43:658-770 - samples
This data set contains next generation sequencing (NGS) data of two serial tumor samples (primary and a metastasis) from a patient with colorectal cancer showing an ERBB2 c.2264T>C (p.Leu755Ser). NGS was performed using the Illumina TruSeq Amplicon Cancer Panel (TSACP, Illumina) covering 212 amplic...
EGAD00001002252 | EGA
GenomicsIntegrated Molecular Profilting in Advanced Cancers Trial
The present protocol seeks to provide molecular profiling data to the treating physician for patients with advanced breast, non-small cell lung, colorectal, genitourinary, pancreatobiliary gastrointestinal, upper aerodigestive tract, gynecological, melanoma, unknown primary, and rare carcinomas, as ...
EGAS00001001897 | EGA
GenomicsUHN Genomics Data Access Committee
Data Access Committee EGAC00001000912
EGAC00001000912 | EGA
UnknownTranscription factors orchestrate dynamic interplay between genome topology and gene regulation during cell reprogramming.
Not available
S-EPMC5810905 | biostudies-literature
UnknownBRCA2 Germline Mutations Identify Gastric Cancers Responsive to PARP Inhibitors.
Not available
S-EPMC10183806 | biostudies-literature
GenomicsDown syndrome SNPs - samples
Down syndrome SNP genotyping data
EGAD00010000464 | EGA
GenomicsDown syndrome CNVs - samples
Down syndrome CNV genotyping data
EGAD00010000466 | EGA
GenomicsThe complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome
Here we aimed to contribute to the description of the genetic architecture of Congenital heart defect (CHD) in Down syndrome (DS), and report the results of a genome-wide association study using samples from DS individuals with and without CHD. CHD is a common developmental defect of DS occurring in...
EGAS00000000129 | EGA
Sort   by:  
 Page size