Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

ABSTRACT: Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants

PROVIDER: PRJNA360024 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
	SRR5140480_1.fastq.gz	Fastqsanger.gz
	SRR5140480_2.fastq.gz	Fastqsanger.gz
	SRR5140490.fastq.gz	Fastqsanger.gz
	SRR5140500.fastq.gz	Fastqsanger.gz
	SRR5140510.fastq.gz	Fastqsanger.gz

Items per page:

1 - 5 of 724

Similar Datasets

Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach

Project description:In order to provide a faster, more comprehensive and cost effective assay, we constructed a DNA fluidic array, CapitalBioMiamiOtoArray, for the detection of sequence variants in five genes that are common in most populations of European descent. Our results show 100% concordance between the fluidic array biochip-based approach and the established Sanger sequencing method, thus proving its robustness and reliability at a relatively low cost.

2017-02-17 | GSE94994 | GEO

Project description:A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

| PRJNA135881 | ENA

Homo sapiens

Project description:A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (Human1Mv1_C)

| PRJNA139749 | ENA

Homo sapiens

Project description:A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (1X1M)

| PRJNA139829 | ENA

Homo sapiens

Project description:A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (GenomeWideSNP_6)

| PRJNA139827 | ENA

Homo sapiens

Project description:A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (WGTP)

| PRJNA139405 | ENA

Homo sapiens

Project description:A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (Mapping250K_Nsp)

| PRJNA139691 | ENA

Homo sapiens

Project description:A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (244A)

| PRJNA139833 | ENA

Homo sapiens

Project description:A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (2X244K)

| PRJNA139547 | ENA

Homo sapiens

Project description:A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (Illumina_650Y)

| PRJNA139685 | ENA

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data