BACKGROUND: The recent advancements in high-throughput sequencing have resulted in the availability of annotated genomes, as well as of multi-omics data for many living organisms. This has increased the need for graphic tools that allow the concurrent visualization of genomes and feature-associated multi-omics data on single publication-ready plots. RESULTS: We present chromoMap, an R package, developed for the construction of interactive visualizations of chromosomes/chromosomal regions, mapping of any chromosomal feature with known coordinates (i.e., protein coding genes, transposable elements, non-coding RNAs, microsatellites, etc.), and chromosomal regional characteristics (i.e. genomic feature density, gene expression, DNA methylation,...
BackgroundBiological studies involve a growing number of distinct high-throughput experiments to cha...
The pace of the sequencing and computational assembly of novel reference genomes is accelerating. Th...
International audienceBackgroundDetection of large genomic rearrangements, such as large indels, dup...
BACKGROUND: The recent advancements in high-throughput sequencing have resulted in the availability ...
The new tools used to explore the human genome produce an enormous amount of data. This data has to ...
Summary: ChromoWheel is an Internet browser application for generating whole-genome illustrations. I...
Long-range chromosomal associations between genomic regions, and their repositioning in the 3D space...
Precise quantitative and spatiotemporal control of gene expression is necessary to ensure proper cel...
Altres ajuts: Plan Estatal de I+D+I 2013-16; Asociación Española Contra en CáncerAbstract. Motivatio...
We present an interactive web application for visualizing genomic data of prokaryotic chro-mosomes. ...
Abstract Background Comparative genomics has become a significant research area in recent years, fol...
The representation, integration, and interpretation of omic data is a complex task, in particular co...
<div><p>Single-nucleotide polymorphism (SNP) is one of the most common sources of genetic variations...
100 species from 42 families. The blue coloured families represent at least one species from the fam...
100 species from 42 families. The blue coloured families represent at least one species from the fam...
BackgroundBiological studies involve a growing number of distinct high-throughput experiments to cha...
The pace of the sequencing and computational assembly of novel reference genomes is accelerating. Th...
International audienceBackgroundDetection of large genomic rearrangements, such as large indels, dup...
BACKGROUND: The recent advancements in high-throughput sequencing have resulted in the availability ...
The new tools used to explore the human genome produce an enormous amount of data. This data has to ...
Summary: ChromoWheel is an Internet browser application for generating whole-genome illustrations. I...
Long-range chromosomal associations between genomic regions, and their repositioning in the 3D space...
Precise quantitative and spatiotemporal control of gene expression is necessary to ensure proper cel...
Altres ajuts: Plan Estatal de I+D+I 2013-16; Asociación Española Contra en CáncerAbstract. Motivatio...
We present an interactive web application for visualizing genomic data of prokaryotic chro-mosomes. ...
Abstract Background Comparative genomics has become a significant research area in recent years, fol...
The representation, integration, and interpretation of omic data is a complex task, in particular co...
<div><p>Single-nucleotide polymorphism (SNP) is one of the most common sources of genetic variations...
100 species from 42 families. The blue coloured families represent at least one species from the fam...
100 species from 42 families. The blue coloured families represent at least one species from the fam...
BackgroundBiological studies involve a growing number of distinct high-throughput experiments to cha...
The pace of the sequencing and computational assembly of novel reference genomes is accelerating. Th...
International audienceBackgroundDetection of large genomic rearrangements, such as large indels, dup...