Genome Biology publishes outstanding research in all areas of biology and biomedicine studied from a genomic and post-genomic perspective. The current impact factor is 10.1 (2023) * and the journal is ranked 3rd among research journals in the Genetics and Heredity category, and 2nd among research...
Genome Biology is a leading open access journal in biology and biomedicine research, with 10.1 Impact Factor and 21 days to first decision. As the ...
Year Impact Factor (IF) Total Articles Total Cites 2023 (2024 update) 6.2 - - 2022 - - 2021 9.438 - 51169 2020 9.043 151 47141 2019 11.093 180 41755 2018 9.944 169 39240 2017 10.101 185 38842 2016 11.922 155 36644 2015 11.351 171 34396 2014 14.630 187 33977 2013 13.852 192 30995 2012...
基因组生物学(Genome Biology)是一本由BioMed Central出版的一本Biochemistry, Genetics and Molecular Biology-Genetics学术刊物,主要报道Biochemistry, Genetics and Molecular Biology-Genetics相关领域研究成果与实践。本刊已入选来源期刊,属于国际一流期刊。该刊创刊于2000年,出版周期Monthly。2021-2022年最新版WOS分区等级...
Citation Impact 2023 Journal Impact Factor: 10.4 5-year Journal Impact Factor: 12.6 Source Normalized Impact per Paper (SNIP): 2.375 SCImago Journal Rank (SJR): 4.975 Speed 2024 Submission to first editorial decision (median days): 8
K-mer spectra can have many forms and shapes dependent on both biology and the sequencing technique, but let's use an idealised case - a k-mer spectra, that does not have any sequencing errors, or repetitive DNA. It has been manually constructed from a k-mer spectra ofTimema cristinae(...
Predicting the effects of coding variants is a major challenge. While recent deep-learning models have improved variant effect prediction accuracy, they cannot analyze all coding variants due to dependency on close homologs or software limitations. Here
Volume 6, article number 697, (2023) Cite this article Download PDF You have full access to this open access article Communications Biology Hiroki Ban, Shinya Sato, Shinya Yoshikawa, Kazumasa Yamada, Yoji Nakamura, Mutsuo Ichinomiya, Naoki Sato, Romain Blanc-Mathieu, Hisashi Endo, ...
heritability estimates ranging from 17% to 28%, our research revealed that a sizable portion of the LVRWT phenotypic variability is explained by the underlying genetics. Furthermore, the modest genetic correlations and limited locus overlap of the 12 LVRWT traits highlighted their distinct biology....
Genome Biology volume 24, Article number: 53 (2023) Cite this article 5399 Accesses 8 Altmetric Metrics details Abstract Background Alternative splicing is a widespread regulatory phenomenon that enables a single gene to produce multiple transcripts. Among the different types of alternative splicing, ...