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期刊名:Genome biology

缩写:GENOME BIOL

ISSN:1474-760X

e-ISSN:1474-760X

IF/分区:9.4/Q1

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共收录本刊相关文章索引6455
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Marc Horlacher,Nils Wagner,Lambert Moyon et al. Marc Horlacher et al.
We present RBPNet, a novel deep learning method, which predicts CLIP-seq crosslink count distribution from RNA sequence at single-nucleotide resolution. By training on up to a million regions, RBPNet achieves high generalization on eCLIP, i...
Dongya Wu,Lingjuan Xie,Yanqing Sun et al. Dongya Wu et al.
Background: Asian rice is one of the world's most widely cultivated crops. Large-scale resequencing analyses have been undertaken to explore the domestication and de-domestication genomic history of Asian rice, but the ev...
Saba Ghaffari,Kelly J Bouchonville,Ehsan Saleh et al. Saba Ghaffari et al.
Differential gene expression in bulk transcriptomics data can reflect change of transcript abundance within a cell type and/or change in the proportions of cell types. Expression deconvolution methods can help differentiate these scenarios....
Francisco Avila Cobos,Mohammad Javad Najaf Panah,Jessica Epps et al. Francisco Avila Cobos et al.
Background: RNA profiling technologies at single-cell resolutions, including single-cell and single-nuclei RNA sequencing (scRNA-seq and snRNA-seq, scnRNA-seq for short), can help characterize the composition of tissues a...
Sergio Villicaña,Juan Castillo-Fernandez,Eilis Hannon et al. Sergio Villicaña et al.
Background: Pinpointing genetic impacts on DNA methylation can improve our understanding of pathways that underlie gene regulation and disease risk. Resul...
Jingwen Ren,Bida Gu,Mark J P Chaisson Jingwen Ren
Roughly 3% of the human genome is composed of variable-number tandem repeats (VNTRs): arrays of motifs at least six bases. These loci are highly polymorphic, yet current approaches that define and merge variants based on alignment breakpoin...
Hao Feng,Guanqun Meng,Tong Lin et al. Hao Feng et al.
We propose a statistical framework ISLET to infer individual-specific and cell-type-specific transcriptome reference panels. ISLET models the repeatedly measured bulk gene expression data, to optimize the usage of shared information within ...
Ireneusz Stolarek,Michal Zenczak,Luiza Handschuh et al. Ireneusz Stolarek et al.
Background: The appearance of Slavs in East-Central Europe has been the subject of an over 200-year debate driven by two conflicting hypotheses. The first assumes that Slavs came to the territory of contemporary Poland no...
Marena Trinidad,Xinying Hong,Steven Froelich et al. Marena Trinidad et al.
Background: Metachromatic leukodystrophy (MLD) is a lysosomal storage disorder caused by mutations in the arylsulfatase A gene (ARSA) and categorized into three subtypes according to age of onset. The functional effect of...
Zhiheng Liu,Giovanni Quinones-Valdez,Ting Fu et al. Zhiheng Liu et al.
Although long-read RNA-seq is increasingly applied to characterize full-length transcripts it can also enable detection of nucleotide variants, such as genetic mutations or RNA editing sites, which is significantly under-explored. Here, we ...