Results 271 to 280 of about 531,444 (314)

Chromosome-level genome assembly of Utricularia aurea Lour., a canivorious higher plant with minute genome. [PDF]

Sci Data
Yu J, Li S, Dong H.
europepmc   +1 more source

Complete genome sequence of <i>Leclercia adecarboxylata</i> strain TB492 isolated from flue-cured tobacco leaves. [PDF]

Microbiol Resour Announc
Liu C, Wang Z, Zhang J, Han L, Wei J, Song K, Yang H, Zang Z, Gao Y, Wang L, Jiang T, Ran S.   +11 more
europepmc   +1 more source

Pylluminator: fast and scalable analysis of DNA methylation data in Python. [PDF]

Bioinform Adv
Fanchon E, Loire B, Trani JP, Magdinier F, Baudot A.   +4 more
europepmc   +1 more source

Shotgun metagenomic dataset of leaf endophytic microbiome of the garden sage (Salvia officinalis L.). [PDF]

BMC Genom Data
Palanisamy M, Babalola OO, Ramalingam S.
europepmc   +1 more source

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Illumina, Inc.

Pharmacogenomics, 2005
Illumina, Inc., based in San Diego (CA, USA), is a genomics tool company that develops and markets integrated array-based systems and assays for a broad range of applications including genotyping, gene expression and epigenetics. Product offerings range from focused assay sets (up to 1,536 multiplexed assays) to whole-genome analysis (>100,000 assays ...
Frank J, Steemers, Kevin L, Gunderson
openaire   +2 more sources

Best Practices for Illumina Library Preparation

Current Protocols in Human Genetics, 2019
AbstractIn this unit, we describe a set of protocols and recommendations for Illumina library preparation. We review best practices in template quantitation methods; template fragmentation methodologies; solid‐phase reverse‐immobilization cleanup, including buffer exchange and size selection; end repair, A‐tailing, and adapter ligation; indexing ...
Iraad F, Bronner, Michael A, Quail
openaire   +2 more sources

ANALYSIS OF CONTEXT-DEPENDENT ERRORS FOR ILLUMINA SEQUENCING

Journal of Bioinformatics and Computational Biology, 2012
The new generation of short-read sequencing technologies requires reliable measures of data quality. Such measures are especially important for variant calling. However, in the particular case of SNP calling, a great number of false-positive SNPs may be obtained. One needs to distinguish putative SNPs from sequencing or other errors. We found that not
Irina I. Abnizova, Steven Leonard, Tom Skelly, Andy Brown, David K. Jackson, Marina Gourtovaia, Guoying Qi, Rene te Boekhorst, Nadeem Faruque, Kevin Lewis, Tony Cox 0001   +10 more
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Genotype Calling for the Illumina Platform

2011
Genome-wide association studies have been made possible because of advancements in the design of genotyping technologies to assay a million or more single nucleotide polymorphisms (SNPs) simultaneously. This has resulted in the introduction of automated and unsupervised statistical approaches for translating the probe hybridization intensities into the
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Ombra, che illumina.

2023
"Lunario" is one of Guidi's last books. This is undoubtedly the artist's least characteristic work – an unusual project for a photographer of streets and sites of memory, of the outskirts and of domestic spaces. Here Guidi - a visual phenomenologist of the surroundings, the variations in the appearances of which he explores in precise intervals of time
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