Example of Mammalian Genome format
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Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format
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Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format Example of Mammalian Genome format
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open access Open Access ISSN: 9388990 e-ISSN: 14321777

Mammalian Genome — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Genetics #114 of 325 up up by 9 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 171 Published Papers | 918 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 05/07/2020
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Top papers
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FAQ

Journal Performance & Insights

  • Impact Factor
  • CiteRatio
  • SJR
  • SNIP

Impact factor determines the importance of a journal by taking a measure of frequency with which the average article in a journal has been cited in a particular year.

2.287

2% from 2018

Impact factor for Mammalian Genome from 2016 - 2019
Year Value
2019 2.287
2018 2.343
2017 2.687
2016 2.509
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 2% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

CiteRatio is a measure of average citations received per peer-reviewed paper published in the journal.

5.4

15% from 2019

CiteRatio for Mammalian Genome from 2016 - 2020
Year Value
2020 5.4
2019 4.7
2018 4.5
2017 4.9
2016 3.8
graph view Graph view
table view Table view

insights Insights

  • CiteRatio of this journal has increased by 15% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

SCImago Journal Rank (SJR) measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

1.186

10% from 2019

SJR for Mammalian Genome from 2016 - 2020
Year Value
2020 1.186
2019 1.082
2018 1.704
2017 1.647
2016 1.42
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 10% in last years.
  • This journal’s SJR is in the top 10 percentile category.

Source Normalized Impact per Paper (SNIP) measures actual citations received relative to citations expected for the journal's category.

0.772

29% from 2019

SNIP for Mammalian Genome from 2016 - 2020
Year Value
2020 0.772
2019 0.599
2018 0.717
2017 0.708
2016 0.685
graph view Graph view
table view Table view

insights Insights

  • SNIP of this journal has increased by 29% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

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CiteRatio: 7.3 | SJR: 2.628 | SNIP: 1.713
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Mammalian Genome

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Springer

Mammalian Genome

Mammalian Genome is devoted to studies of mammalian genomics and genetics, serving as a vehicle for the dissemination of work in the emerging field of functional genomics. Mammalian Genome focuses on the experimental, theoretical, and technical aspects of genomics and genetics...... Read More

Genetics

Biochemistry, Genetics and Molecular Biology

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Last updated on
05 Jul 2020
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ISSN
0938-8990
i
Impact Factor
Medium - 0.808
i
Open Access
No
i
Sherpa RoMEO Archiving Policy
Green faq
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Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
SPBASIC
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Citation Type
Author Year
(Blonder et al, 1982)
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Bibliography Example
Beenakker CWJ (2006) Specular andreev reflection in graphene. Phys Rev Lett 97(6):067,007, URL 10.1103/PhysRevLett.97.067007

Top papers written in this journal

Journal Article DOI: 10.1007/S00335-001-1016-3
Map Manager QTX, cross-platform software for genetic mapping.
Kenneth F. Manly1, Robert H. Cudmore1, Jane M. Meer1
01 Dec 2001 - Mammalian Genome

Abstract:

Map Manager QTX (QTX) is software for analysis of genetic mapping experiments in experimental plants and animals. It includes functions for mapping both Mendelian and quantitative trait loci. QTX is an enhanced version of Map Manager QT, rewritten with the aid of cross-platform libraries (XVT, Boulder Software Foundry, Inc.),... Map Manager QTX (QTX) is software for analysis of genetic mapping experiments in experimental plants and animals. It includes functions for mapping both Mendelian and quantitative trait loci. QTX is an enhanced version of Map Manager QT, rewritten with the aid of cross-platform libraries (XVT, Boulder Software Foundry, Inc.), which allow it to be compiled for multiple computer platforms. It currently is distributed for Microsoft Windows and Mac OS and is available at http://mapmgr.roswellpark.org/mmQTX.html. read more read less

Topics:

Software (51%)51% related to the paper, Cross-platform (51%)51% related to the paper
1,237 Citations
Journal Article DOI: 10.1007/S003359900171
Interpreting cDNA sequences: Some insights from studies on translation
Marilyn Kozak1
01 Aug 1996 - Mammalian Genome

Abstract:

This review discusses some rules for assessing the completeness of a cDNA sequence and identifying the start site for translation. Features commonly invoked-such as an ATG codon in a favorable context for initiation, or the presence of an upstream in-frame terminator codon, or the prediction of a signal peptide-like sequence ... This review discusses some rules for assessing the completeness of a cDNA sequence and identifying the start site for translation. Features commonly invoked-such as an ATG codon in a favorable context for initiation, or the presence of an upstream in-frame terminator codon, or the prediction of a signal peptide-like sequence at the amino terminus-have some validity; but examples drawn from the literature illustrate limitations to each of these criteria. The best advice is to inspect a cDNA sequence not only for these positive features but also for the absence of certain negative indicators. Three specific warning signs are discussed and documented: (i) The presence of numerous ATG codons upstream from the presumptive start site for translation often indicates an aberration (sometimes a retained intron) at the 5' end of the cDNA. (ii) Even one strong, upstream, out-of-frame ATG codon poses a problem if the reading frame set by the upstream ATG overlaps the presumptive start of the major open reading frame. Many cDNAs that display this arrangement turn out to be incomplete; that is, the out-of-frame ATG codon is within, rather than upstream from, the protein coding domain. (iii) A very weak context at the putative start site for translation often means that the cDNA lacks the authentic initiator codon. In addition to presenting some criteria that may aid in recognizing incomplete cDNA sequences, the review includes some advice for using in vitro translation systems for the expression of cDNAs. Some unresolved questions about translational regulation are discussed by way of illustrating the importance of verifying mRNA structures before making deductions about translation. read more read less

Topics:

Open reading frame (59%)59% related to the paper, Start codon (58%)58% related to the paper, Five prime untranslated region (58%)58% related to the paper, Shine-Dalgarno sequence (56%)56% related to the paper
756 Citations
Journal Article DOI: 10.1007/S003359900551
Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment
01 Oct 1997 - Mammalian Genome

Abstract:

For an understanding of the aberrant biology seen in mouse mutations and identification of more subtle phenotype variation, there is a need for a full clinical and pathological characterization of the animals. Although there has been some use of sophisticated techniques, the majority of behavioral and functional analyses in m... For an understanding of the aberrant biology seen in mouse mutations and identification of more subtle phenotype variation, there is a need for a full clinical and pathological characterization of the animals. Although there has been some use of sophisticated techniques, the majority of behavioral and functional analyses in mice have been qualitative rather than quantitative in nature. There is, however, no comprehensive routine screening and testing protocol designed to identify and characterize phenotype variation or disorders associated with the mouse genome. We have developed the SHIRPA procedure to characterize the phenotype of mice in three stages. The primary screen utilizes standard methods to provide a behavioral and functional profile by observational assessment. The secondary screen involves a comprehensive behavioral assessment battery and pathological analysis. These protocols provide the framework for a general phenotype assessment that is suitable for a wide range of applications, including the characterization of spontaneous and induced mutants, the analysis of transgenic and gene-targeted phenotypes, and the definition of variation between strains. The tertiary screening stage described is tailored to the assessment of existing or potential models of neurological disease, as well as the assessment of phenotypic variability that may be the result of unknown genetic influences. SHIRPA utilizes standardized protocols for behavioral and functional assessment that provide a sensitive measure for quantifying phenotype expression in the mouse. These paradigms can be refined to test the function of specific neural pathways, which will, in turn, contribute to a greater understanding of neurological disorders. read more read less

Topics:

SHIRPA (60%)60% related to the paper
754 Citations
Journal Article DOI: 10.1007/BF00389540
Maps from two interspecific backcross DNA panels available as a community genetic mapping resource
01 May 1994 - Mammalian Genome

Abstract:

We established two mouse interspecific backcross DNA panels, one containing 94 N2 animals from the cross (C57BL/6J × Mus spretus)F1 × C57BL/6J, and another from 94 N2 animals from the reciprocal backcross (C57BL/6J × SPRET/Ei)F1 × SPRET/Ei. We prepared large quantities of DNA from most tissues of each animal to create a commu... We established two mouse interspecific backcross DNA panels, one containing 94 N2 animals from the cross (C57BL/6J × Mus spretus)F1 × C57BL/6J, and another from 94 N2 animals from the reciprocal backcross (C57BL/6J × SPRET/Ei)F1 × SPRET/Ei. We prepared large quantities of DNA from most tissues of each animal to create a community resource of interspecific backcross DNA for use by laboratories interested in mapping loci in the mouse. Initial characterization of the genetic maps of both panels has been completed. We used MIT SSLP markers, proviral loci, and several other sequence-defined genes to anchor our maps to other published maps. The BSB panel map (from the backcross to C57BL/6J) contains 215 loci and is anchored by 45 SSLP and 32 gene sequence loci. The BSS panel map (from the backcross to SPRET/Ei) contains 451 loci and is anchored by 49 SSLP loci, 43 proviral loci, and 60 gene sequence loci. To obtain a high density of markers, we used motif-primed PCR to “fingerprint” the panel DNAs. We constructed two maps, each representing one of the two panels. All new loci can be located with a high degree of certainty on the maps at current marker density. Segregation patterns in these data reveal several examples of transmission ratio distortion and permit analysis of the distribution of crossovers on individual chromosomes. read more read less

Topics:

Gene mapping (50%)50% related to the paper
575 Citations
Journal Article DOI: 10.1007/BF00357089
A Macintosh program for storage and analysis of experimental genetic mapping data.
Kenneth F. Manly1
01 Jan 1993 - Mammalian Genome

Abstract:

RI Manager (Manly and Elliott, 1991) is a microcomputer program to assist genetic mapping in experimental organisms by providing functions for convenient data collection, organization, and analysis. It has been under development since 1988, and new features are constantly being added. This review presents the current capabili... RI Manager (Manly and Elliott, 1991) is a microcomputer program to assist genetic mapping in experimental organisms by providing functions for convenient data collection, organization, and analysis. It has been under development since 1988, and new features are constantly being added. This review presents the current capabilities of the program and some of the principles that are guiding its development. RI Manager was originally developed specifically for data from recombinant inbred strains of mice (Taylor 1989). It has since been extended to analyze data from backcrosses, and it will be extended further to ana lyze F 2 data. To include these additional functions, the program is now being called Map Manager, and this name will be used throughout this review. The functions of Map Manager can be divided, somewhat arbitrarily, into analysis functions and database functions. The database functions are those which allow a user to organize and manipulate mapping data conveniently. The presence of these functions distinguishes Map Manager from other mapping programs. This review will describe the analysis and database functions separately. read more read less

Topics:

Human genetics (50%)50% related to the paper
493 Citations
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Mammalian Genome format uses SPBASIC citation style.

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Frequently asked questions

Absolutely not! With our tool, you can freely write without having to focus on LaTeX. You can write your entire paper as per the Mammalian Genome guidelines and autoformat it.

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Sure. We support all the top citation styles like APA style, MLA style, Vancouver style, Harvard style, Chicago style, etc. For example, in case of this journal, when you write your paper and hit autoformat, it will automatically update your article as per the Mammalian Genome citation style.

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A matter of seconds. Besides that, our intuitive editor saves a load of your time in writing and formating your manuscript.

One little Google search can get you the Word template for any journal. However, why do you need a Word template when you can write your entire manuscript on SciSpace, autoformat it as per Mammalian Genome's guidelines and download the same in Word, PDF and LaTeX formats? Try us out!.

Absolutely! You can do it using our intuitive editor. It's very easy. If you need help, you can always contact our support team.

SciSpace is an online tool for now. We'll soon release a desktop version. You can also request (or upvote) any feature that you think might be helpful for you and the research community in the feature request section once you sign-up with us.

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After you have written and autoformatted your paper, you can download it in multiple formats, viz., PDF, Docx and LaTeX.

To be honest, the answer is NO. The impact factor is one of the many elements that determine the quality of a journal. Few of those factors the review board, rejection rates, frequency of inclusion in indexes, Eigenfactor, etc. You must assess all the factors and then take the final call.

SHERPA/RoMEO Database

We have extracted this data from Sherpa Romeo to help our researchers understand the access level of this journal. The following table indicates the level of access a journal has as per Sherpa Romeo Archiving Policy.

RoMEO Colour Archiving policy
Green Can archive pre-print and post-print or publisher's version/PDF
Blue Can archive post-print (ie final draft post-refereeing) or publisher's version/PDF
Yellow Can archive pre-print (ie pre-refereeing)
White Archiving not formally supported
FYI:
  1. Pre-prints as being the version of the paper before peer review and
  2. Post-prints as being the version of the paper after peer-review, with revisions having been made.

The 5 most common citation types in order of usage are:.

S. No. Citation Style Type
1. Author Year
2. Numbered
3. Numbered (Superscripted)
4. Author Year (Cited Pages)
5. Footnote

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After uploading your paper on SciSpace, you would see a button to request a journal submission service for Mammalian Genome.

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Yes. SciSpace provides this functionality.

After signing up, you would need to import your existing references from Word or .bib file.

SciSpace would allow download of your references in Mammalian Genome Endnote style, according to springer guidelines.

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