Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

ABSTRACT: An in tandem multiilocus Culicoides identification methodology

PROVIDER: PRJNA748077 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
	SRR15194102.fastq.gz	Fastqsanger.gz
	SRR15194737.fastq.gz	Fastqsanger.gz
	SRR15194761.fastq.gz	Fastqsanger.gz
	SRR15194762.fastq.gz	Fastqsanger.gz
	SRR15194763.fastq.gz	Fastqsanger.gz

Items per page:

1 - 5 of 10

Similar Datasets

Project description:An in tandem multiilocus mosquito identification methodology

| PRJNA681030 | ENA

Flash proteotyping of microbial isolates by tandem mass spectrometry

Project description:Flash proteotyping is a methodology for ultra-fast identification of microorganisns by tandem mass spectrometry. Here, we obtained results on five reference strains and ten new bacterial isolates. The methodology is based on direct sample infusion into the mass spectromete and an original, highly sensitive procedure for data processing and taxonomic identification.

2023-12-21 | PXD045510 | Pride

insect metagenome

Project description:Culicoides brevitarsis, Culicoides multimaculatus and Culicoides victoriae, 16S rRNA raw sequence reads

| PRJNA347486 | ENA

Topo-Seq application for topoisomerases binding sites identification with a single-nucleotide resolution

Project description:Topo-Seq is a ChIP-Seq-based methodology that allows high-throughput identification of topoisomerases binding (cleavage) sites with a single-base precision. On a first stage of the project DNA-gyrase binding sites on a Escherichia coli DY330 genome are investigated.

2018-07-17 | GSE117186 | GEO

Culicoides imicola

Project description:Culicoides imicola overview

| PRJNA1156300 | ENA

Culicoides sonorensis

Project description:Culicoides sonorensis overview

| PRJNA435443 | ENA

Single cell chromatin immunocleavage sequencing (scChIC-Seq) to profile histone modification

Project description:We report a single-cell chromatin immunocleavage sequencing (scChIC-seq) methodology for analyzing histone modifications, which involves targeting of the micrococcal nuclease (MNase) by tethering it to an antibody and selective PCR amplification of cleaved target sites. We show that the protocol reliably detects the H3K4me3 and H3K27me3 target sites in single human white blood cells (WBC), resulting data for successful identification of unique blood cell types based on clustering analysis.

2019-03-28 | GSE105012 | GEO

Project description:TANDEM WGS

| PRJNA595834 | ENA

Synthetic plasmid

Project description:tandem-genotypes

| PRJDB7133 | ENA

Project description:Genome assembly of Culicoides stellifer

| PRJNA1112419 | ENA