Results 31 to 40 of about 1,004,545 (280)

Genomic Structural Variations Within Five Continental Populations of Drosophila melanogaster

open access: yesG3: Genes, Genomes, Genetics, 2018
Chromosomal structural variations (SV) including insertions, deletions, inversions, and translocations occur within the genome and can have a significant effect on organismal phenotype. Some of these effects are caused by structural variations containing
Evan Long   +3 more
doaj   +1 more source

Long-read single-molecule maps of the functional methylome [PDF]

open access: yesGenome Research, 2019
We report on the development of a methylation analysis workflow for optical detection of fluorescent methylation profiles along chromosomal DNA molecules. In combination with Bionano Genomics genome mapping technology, these profiles provide a hybrid genetic/epigenetic genome-wide map composed of DNA molecules spanning hundreds of kilobase pairs.
Hila Sharim   +25 more
openaire   +5 more sources

Nanopore sequencing unveils the complexity of the cold-activated murine brown adipose tissue transcriptome

open access: yesiScience, 2023
Summary: Alternative transcription increases transcriptome complexity by expression of multiple transcripts per gene. Annotation and quantification of transcripts using short-read sequencing is non-trivial.
Christoph Andreas Engelhard   +4 more
doaj   +1 more source

Chromosomal-level assembly of the Asian Seabass genome using long sequence reads and multi-layered scaffolding [PDF]

open access: yes, 2016
We report here the ~670 Mb genome assembly of the Asian seabass (Lates calcarifer), a tropical marine teleost. We used long-read sequencing augmented by transcriptomics, optical and genetic mapping along with shared synteny from closely related fish ...
A Bairoch   +190 more
core   +5 more sources

Jabba: hybrid error correction for long sequencing reads [PDF]

open access: yes, 2016
Background: Third generation sequencing platforms produce longer reads with higher error rates than second generation technologies. While the improved read length can provide useful information for downstream analysis, underlying algorithms are ...
Audenaert, P.   +6 more
core   +3 more sources

SOAP3-dp: Fast, Accurate and Sensitive GPU-based Short Read Aligner [PDF]

open access: yes, 2013
To tackle the exponentially increasing throughput of Next-Generation Sequencing (NGS), most of the existing short-read aligners can be configured to favor speed in trade of accuracy and sensitivity. SOAP3-dp, through leveraging the computational power of
Chang Yu   +16 more
core   +8 more sources

Structural variant calling: the long and the short of it

open access: yesGenome Biology, 2019
Recent research into structural variants (SVs) has established their importance to medicine and molecular biology, elucidating their role in various diseases, regulation of gene expression, ethnic diversity, and large-scale chromosome evolution—giving ...
Medhat Mahmoud   +5 more
doaj   +1 more source

S-conLSH: alignment-free gapped mapping of noisy long reads [PDF]

open access: yesBMC Bioinformatics, 2019
Abstract Background The advancement of SMRT technology has unfolded new opportunities of genome analysis with its longer read length and low GC bias. Alignment of the reads to their appropriate positions in the respective reference genome is the first but costliest step of any analysis pipeline
Chakraborty, Angana   +5 more
openaire   +5 more sources

A whole-genome shotgun approach for assembling and anchoring the hexaploid bread wheat genome [PDF]

open access: yes, 2015
Citation: Chapman, J. A., Mascher, M., Buluç, A., Barry, K., Georganas, E., Session, A., . . . Rokhsar, D. S. (2015). A whole-genome shotgun approach for assembling and anchoring the hexaploid bread wheat genome. Genome Biology, 16(1). doi:10.1186/s13059-
A Graner   +83 more
core   +5 more sources

Sequencing and de novo assembly of 150 genomes from Denmark as a population reference [PDF]

open access: yes, 2017
Hundreds of thousands of human genomes are now being sequenced to characterize genetic variation and use this information to augment association mapping studies of complex disorders and other phenotypic traits.
A Helgason   +106 more
core   +3 more sources

Home - About - Disclaimer - Privacy