首页 文献索引 SCI期刊 AI助手
期刊目录筛选

期刊名:Genome biology

缩写:GENOME BIOL

ISSN:1474-760X

e-ISSN:1474-760X

IF/分区:9.4/Q1

文章目录 更多期刊信息

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
Pei Lu,Jie Yang,Mao Li et al. Pei Lu et al.
Background: Extensive studies have revealed the function and mechanism of lncRNAs in development and differentiation, but the majority have focused on those lncRNAs adjacent to protein-coding genes. In contrast, lncRNAs l...
Georgi K Marinov,Samuel H Kim,S Tansu Bagdatli et al. Georgi K Marinov et al.
Detecting and mitigating off-target activity is critical to the practical application of CRISPR-mediated genome and epigenome editing. While numerous methods have been developed to map Cas9 binding specificity genome-wide, they are generall...
Xiaotang Wang,Wei Fan,Na Li et al. Xiaotang Wang et al.
Background: Ocular neovascularization is a leading cause of blindness. Retinal microglia have been implicated in hypoxia-induced angiogenesis and vasculopathy, but the underlying mechanisms are not entirely clear. Lactyla...
Gerard A Bouland,Ahmed Mahfouz,Marcel J T Reinders Gerard A Bouland
With the number of cells measured in single-cell RNA sequencing (scRNA-seq) datasets increasing exponentially and concurrent increased sparsity due to more zero counts being measured for many genes, we demonstrate here that downstream analy...
Ian Hoskins,Song Sun,Atina Cote et al. Ian Hoskins et al.
The impact of millions of individual genetic variants on molecular phenotypes in coding sequences remains unknown. Multiplexed assays of variant effect (MAVEs) are scalable methods to annotate relevant variants, but existing software lacks ...
Rene Snajder,Adrien Leger,Oliver Stegle et al. Rene Snajder et al.
We present pycoMeth, a toolbox to store, manage and analyze DNA methylation calls from long-read sequencing data obtained using the Oxford Nanopore Technologies sequencing platform. Building on a novel, rapid-access, read-level and referenc...
Joseph D Janizek,Anna Spiro,Safiye Celik et al. Joseph D Janizek et al.
As interest in using unsupervised deep learning models to analyze gene expression data has grown, an increasing number of methods have been developed to make these models more interpretable. These methods can be separated into two groups: p...
Jacob Schreiber,Carles Boix,Jin Wook Lee et al. Jacob Schreiber et al.
A promising alternative to comprehensively performing genomics experiments is to, instead, perform a subset of experiments and use computational methods to impute the remainder. However, identifying the best imputation methods and what meas...