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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6621
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
Lihua Zhang,Chao He,Yuting Lai et al. Lihua Zhang et al.
Background: Homoeologs are defined as homologous genes resulting from allopolyploidy. Bread wheat, Triticum aestivum, is an allohexaploid species with many homoeologs. Homoeolog expression bias, referring to the relative ...
Sonali Narang,Nikki A Evensen,Jason Saliba et al. Sonali Narang et al.
Background: The NSD2 p.E1099K (EK) mutation is shown to be enriched in patients with relapsed acute lymphoblastic leukemia (ALL), indicating a role in clonal evolution and drug resistance. ...
Mourdas Mohamed,François Sabot,Marion Varoqui et al. Mourdas Mohamed et al.
Transposable Element MOnitoring with LOng-reads (TrEMOLO) is a new software that combines assembly- and mapping-based approaches to robustly detect genetic elements called transposable elements (TEs). Using high- or low-quality genome assem...
Zhe Weng,Fengying Ruan,Weitian Chen et al. Zhe Weng et al.
Epigenetic modifications of histones are associated with development and pathogenesis of disease. Existing approaches cannot provide insights into long-range interactions and represent the average chromatin state. Here we describe BIND&MODI...
Natasha K Tuano,Jonathan Beesley,Murray Manning et al. Natasha K Tuano et al.
Background: Genome-wide association studies (GWAS) have identified > 200 loci associated with breast cancer risk. The majority of candidate causal variants are in non-coding regions and likely modulate cancer risk by regu...
Helena L Crowell,Sarah X Morillo Leonardo,Charlotte Soneson et al. Helena L Crowell et al.
Background: With the emergence of hundreds of single-cell RNA-sequencing (scRNA-seq) datasets, the number of computational tools to analyze aspects of the generated data has grown rapidly. As a result, there is a recurrin...
Wanchao Zhu,Xinxin Miao,Jia Qian et al. Wanchao Zhu et al.
Background: Maize (Zea mays L.) is one of the most important crops worldwide. Although sophisticated maize gene regulatory networks (GRNs) have been constructed for functional genomics and phenotypic dissection, a multi-o...
Iman Hajirasouliha,Stefan Semrau Iman Hajirasouliha
The annual Genome Informatics conference was held at the Wellcome Genome Campus on September 21-23, 2022. The conference covered a remarkable range of topics of which we highlight a few in this report. ...
Shenghan Gao,Xiaofei Yang,Hongtao Guo et al. Shenghan Gao et al.
Significant improvements in long-read sequencing technologies have unlocked complex genomic areas, such as centromeres, in the genome and introduced the centromere annotation problem. Currently, centromeres are annotated in a semi-manual wa...
Alexander Karollus,Thomas Mauermeier,Julien Gagneur Alexander Karollus
Background: The largest sequence-based models of transcription control to date are obtained by predicting genome-wide gene regulatory assays across the human genome. This setting is fundamentally correlative, as those mod...