BMC Genomics citation style guide with bibliography and in-text referencing examples: Journal articles Books Book chapters Reports Web pages. PLUS: Download citation style files for your favorite reference manager.
The 20 articles in this supplement cover mainly "genomic" topics, with three medically-oriented papers going into BMC Medical Genomics for the first time. The InCoB2014 BMC Bioinformatics supplement [ 5 ] comprises 16 manuscripts while another 11 papers are presented in the BMC Systems Biology supplement [ 6 ].
Duration of Peer Review: 1.0 month(s) Result: Accepted directly Write a review: Reviewed 2017-01-20 09:58:48 BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. Show Review in Original Language (2) Thank | Z: Author: bababa Subject Area: Life Journals in the field of genomics are relatively easy, especially the annual supplement(The article selected by the meeting) is very easy.In addition to supplements, articles in other issues are generally slow to review, and even after a month, manuscript numbers are given. BMC Genomics | Acceptance Rate. The acceptance rate for an academic journal is dependent upon the relative demand for publishing in a particular journal, the peer review processes in place, the mix of invited and unsolicited submissions, and time to publication, among others. The BMC Genomics Impact Factor IF measures the average number of citations received in a particular year (2020) by papers published in the BMC Genomics during the two preceding years (2018-2019). Note that 2020 Impact Factor are reported in 2021; they cannot be calculated until all of the 2020 publications have been processed by the indexing BMC Genomic Data, previously known as BMC Genetics, is an open-access, peer-reviewed journal that welcomes submissions that describe genomic and genetic research data, report new analyses of genomic data and introduce community databases. We promote open science through the sharing of data.
Bmc BioMed Central (BMC) is a United Kingdom-based, for-profit scientific open access publisher With currently 70 BMC journals operating fully open peer review. BMC Family Practice; BMC Gastroenterology; BMC Genetics; BMC Genomics&nb BMC Genomics. Modeling Central We thank the editor and the reviewers for their time and effort in providing valuable writing and revision of the manuscript . BMC Genomics is a journal covering the technologies/fields/categories related to Biotechnology (Q1); Genetics (Q1).
BMC Genomics operates a single-blind peer-review system, where the reviewers are aware of the names Please do let us know if you need additional time. 20 Mar 2008 BMC Genomics 2008, 9(Suppl 1):I1 doi:10.1186/1471-2164-9-S1-I1 time and effort in reviewing the submitted manuscripts.
BMC Genomics is a journal covering the technologies/fields/categories related to Biotechnology (Q1); Genetics (Q1). journal/author has published h papers that have each been cited at least h number of times. Nature Reviews Genetic
Volumes and issues. Volume 22 December 2021. December 2021, issue 1; Volume 21 March - December 2020.
Draft genome sequences of strains Salinicola socius SMB35T, Salinicola sp. MH3R3–1 and Chromohalobacter BMC Genetics. 2016. Article.
BMC Genomics: 12.6 weeks: 23.9 weeks: n/a: 4: 3 (good) 1 (bad) Accepted Reviewers recruited by Research Square are paid a small honorarium for completing the review within a specified timeframe. Honoraria are paid regardless of the reviewer recommendation. BMC Genomics operates a single-blind peer-review system, where the reviewers are aware of the names and affiliations of the authors, but the reviewer reports provided to authors are anonymous.
1859, 2006 Optimized time alignment algorithm for LC− MS data: correlation optimized warping using component detection algorithm-selected mass Dynamic metabolomic data analysis: a tutorial review. My main project involved whole genome sequencing and assembly of the wolverine (Gulo gulo) genome. And I was also During this time I worked in various projects at the Department of Population Biology. I performed lab BMC Genomics 15 (1):180. Ekblom R (2009) Book review: The wisdom of birds (Birkhead T).
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Volumes and issues. Volume 22 December 2021. December 2021, issue 1; Volume 21 March - December 2020. December 2020 The 20 articles in this supplement cover mainly "genomic" topics, with three medically-oriented papers going into BMC Medical Genomics for the first time.
BMC Genomics (ISSN 1471-2164) is indexed/tracked/covered by PubMed, MEDLINE, BIOSIS, CAS, EMBASE, Scopus, Zoological Record, Thomson Reuters (ISI) and Google Scholar.
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Journals in the field of genomics are relatively easy, especially the annual supplement(The article selected by the meeting) is very easy.In addition to supplements, articles in other issues are generally slow to review, and even after a month, manuscript numbers are given.
Search. Volumes and issues. Volume 22 December 2021.
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Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: a case report. Merosin-deficient congenital muscular dystrophy type 1A (MDC1A) is a rare autosomal recessive genetic condition caused by deleterious mutations in the LAMA2 gene encoding the laminin-α2 chain.
The BMC Genomics Impact Factor IF measures the average number of citations received in a particular year (2020) by papers published in the BMC Genomics during the two preceding years (2018-2019). Note that 2020 Impact Factor are reported in 2021; they cannot be calculated until all of the 2020 publications have been processed by the indexing BMC Genomic Data, previously known as BMC Genetics, is an open-access, peer-reviewed journal that welcomes submissions that describe genomic and genetic research data, report new analyses of genomic data and introduce community databases. We promote open science through the sharing of data. The BMC Medical Genomics Journal Impact IF 2020-2021 is 2.728. More IF Analysis, Trend, Ranking & Prediction. Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: a case report.