Results 81 to 90 of about 531,444 (314)

Illumina sequence data summary.

open access: yes, 2016
Illumina sequence data summary.
Shea N. Gardner (11724)   +10 more
core   +1 more source

Illumina reads for TA299

open access: yes, 2021
<p>Raw Illumina short reads (~40x) for TA299 Triticum monococcum subsp.
Ibrahim Ahmed, Hanin
core   +1 more source

Longitudinal genome‐wide aneuploidy measurements in circulating cell‐free DNA to predict lack of benefit from pembrolizumab in patients with metastatic urothelial cancer

open access: yesMolecular Oncology, EarlyView.
Many patients with urothelial cancer do not benefit from treatment with pembrolizumab, while at risk of severe side effects. Changes in the levels of circulating tumor DNA early during treatment, measured by a simple and affordable assay that can be easily implemented in the clinic, can be used as a prognostic tool to identify these patients.
Youssra Salhi   +14 more
wiley   +1 more source

Closing the gap: Oxford Nanopore Technologies R10 sequencing allows comparable results to Illumina sequencing for SNP-based outbreak investigation of bacterial pathogens.

open access: yes
Whole-genome sequencing has become the method of choice for bacterial outbreak investigation, with most clinical and public health laboratories currently routinely using short-read Illumina sequencing.
S. Nouws   +11 more
core   +1 more source

Diagnostic applications of next generation sequencing: working towards quality standards [PDF]

open access: yes, 2012
Over the past 6 years, next generation sequencing (NGS) has been established as a valuable high-throughput method for research in molecular genetics and has successfully been employed in the identification of rare and common genetic variations. All major
Klein, Hanns-Georg   +27 more
core   +1 more source

bug and microbe illumina simulated reads

open access: yes, 2021
simulated illumina reads of microbes and subset human genomes as described here: https://hackmd.io/@astrobiomike/generating-in-silico-illumina ...
Michael Lee (4372780)
core   +1 more source

Illumina Onmi

open access: yes, 2009
Illumina recently announced their latest chip for GWA studies - the HumanOmni1-Quad. Generating more than 4 million data points, it assays over 30,000 coding SNPs, contains content derived from the 1000 genomes project, and has probes covering 11,000 common and rare CNVs. I doubt the information gain will immediately be worth the premium price for this
openaire   +1 more source

MITF maintains genome stability in nonmelanocyte lineages

open access: yesMolecular Oncology, EarlyView.
MITF is essential for melanocyte survival and acts as an oncogene in 10%–20% of melanomas. We show that MITF depletion causes genome instability in nonmelanocytic cells, leading to LATS2‐mediated P53 activation, cell cycle arrest, and apoptosis. This study highlights the role of MITF as a genome maintenance factor beyond the melanocyte lineage. Created
Drifa H. Gudmundsdottir   +13 more
wiley   +1 more source

Illumina metagenomics workflow test files

open access: yes, 2021
Test files for my illumina metagenomics ...
Michael Lee (4372780)
core   +1 more source

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