Example of Immunogenetics format
Recent searches

Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format
Sample paper formatted on SciSpace - SciSpace
This content is only for preview purposes. The original open access content can be found here.
Look Inside
Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format Example of Immunogenetics format
Sample paper formatted on SciSpace - SciSpace
This content is only for preview purposes. The original open access content can be found here.
open access Open Access

Immunogenetics — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Genetics #125 of 325 up up by 31 ranks
Immunology #104 of 202 up up by 17 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 227 Published Papers | 1168 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 12/06/2020
Related journals
Insights
General info
Top papers
Popular templates
Get started guide
Why choose from SciSpace
FAQ

Related Journals

open access Open Access
recommended Recommended

PLOS

Quality:  
High
CiteRatio: 11.0
SJR: 3.719
SNIP: 1.882
open access Open Access
recommended Recommended

Nature

Quality:  
High
CiteRatio: 28.2
SJR: 7.305
SNIP: 3.41

NRC Research Press

Quality:  
Good
CiteRatio: 3.7
SJR: 0.635
SNIP: 0.761
open access Open Access

Springer

Quality:  
Medium
CiteRatio: 1.0
SJR: 0.271
SNIP: 0.686

Journal Performance & Insights

Impact Factor

CiteRatio

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.

A measure of average citations received per peer-reviewed paper published in the journal.

2.621

5% from 2018

Impact factor for Immunogenetics from 2016 - 2019
Year Value
2019 2.621
2018 2.492
2017 2.094
2016 2.092
graph view Graph view
table view Table view

5.1

16% from 2019

CiteRatio for Immunogenetics from 2016 - 2020
Year Value
2020 5.1
2019 4.4
2018 4.0
2017 4.0
2016 4.4
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 5% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased by 16% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

Measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

Measures actual citations received relative to citations expected for the journal's category.

1.003

5% from 2019

SJR for Immunogenetics from 2016 - 2020
Year Value
2020 1.003
2019 0.956
2018 1.033
2017 0.916
2016 1.249
graph view Graph view
table view Table view

1.205

21% from 2019

SNIP for Immunogenetics from 2016 - 2020
Year Value
2020 1.205
2019 0.999
2018 0.779
2017 0.654
2016 0.713
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 5% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 21% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Immunogenetics

Guideline source: View

All company, product and service names used in this website are for identification purposes only. All product names, trademarks and registered trademarks are property of their respective owners.

Use of these names, trademarks and brands does not imply endorsement or affiliation. Disclaimer Notice

Springer

Immunogenetics

Immunogenetics publishes original papers, brief communications, and reviews on research in the following areas: immunogenetics of cell interaction, immunogenetics of tissue differentiation and development, phylogeny of alloantigens and of immune response, genetic control of im...... Read More

Genetics

Immunology

Biochemistry, Genetics and Molecular Biology

i
Last updated on
12 Jun 2020
i
ISSN
0093-7711
i
Impact Factor
Medium - 0.762
i
Open Access
Yes
i
Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
i
Endnote Style
Download Available
i
Bibliography Name
SPBASIC
i
Citation Type
Author Year
(Blonder et al, 1982)
i
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/S002510050595
SYFPEITHI: database for MHC ligands and peptide motifs.
Hans-Georg Rammensee1, Jutta Bachmann1, Niels Emmerich1, O. A. Bachor, Stefan Stevanovic1
01 Nov 1999 - Immunogenetics

Abstract:

The first version of the major histocompatibility complex (MHC) databank SYFPEITHI: database for MHC ligands and peptide motifs, is now available to the general public. It contains a collection of MHC class I and class II ligands and peptide motifs of humans and other species, such as apes, cattle, chicken, and mouse, for exa... The first version of the major histocompatibility complex (MHC) databank SYFPEITHI: database for MHC ligands and peptide motifs, is now available to the general public. It contains a collection of MHC class I and class II ligands and peptide motifs of humans and other species, such as apes, cattle, chicken, and mouse, for example, and is continuously updated. All motifs currently available are accessible as individual entries. Searches for MHC alleles, MHC motifs, natural ligands, T-cell epitopes, source proteins/organisms and references are possible. Hyperlinks to the EMBL and PubMed databases are included. In addition, ligand predictions are available for a number of MHC allelic products. The database content is restricted to published data only. read more read less

Topics:

MHC class I (58%)58% related to the paper, Major histocompatibility complex (50%)50% related to the paper
2,406 Citations
Journal Article DOI: 10.1007/BF00172063
MHC ligands and peptide motifs: first listing.
01 Jan 1995 - Immunogenetics

Abstract:

The purpose of this article is to provide a compendium of major histocompatibility complex (MHC) peptide motifs and MHC ligands known to date, together with a discussion of the methods used to gain this information. A problem here is the exponential growth of information in this field over the recent years. The number of know... The purpose of this article is to provide a compendium of major histocompatibility complex (MHC) peptide motifs and MHC ligands known to date, together with a discussion of the methods used to gain this information. A problem here is the exponential growth of information in this field over the recent years. The number of known MHC ligands was zero in 1989 and three in 1990. This article, written in 1994, lists a couple of hundred such ligands, plus a large number of likely ligands. By the time this work is published, we expect a lot more ligands to be known. On the other hand, the peptide motifs of many of the more important MHC class I molecules are known already, so that this article will still be useful as a source of information. For class II, the situation is a bit different. Only a few allele-specific motifs have been reported, and the data from different authors are partially conflicting. The principles of allele-specific ligand motifs, however, have emerged recently by the combination of information on MHC class II structure, ligand sequencing, and peptide binding assays. Thus, these principles can be applied to further ligands to be identified. read more read less
View PDF
1,802 Citations
open accessOpen access Journal Article DOI: 10.1007/S00251-008-0341-Z
NetMHCpan, a method for MHC class I binding prediction beyond humans
01 Jan 2009 - Immunogenetics

Abstract:

Binding of peptides to major histocompatibility complex (MHC) molecules is the single most selective step in the recognition of pathogens by the cellular immune system. The human MHC genomic region (called HLA) is extremely polymorphic comprising several thousand alleles, each encoding a distinct MHC molecule. The potentially... Binding of peptides to major histocompatibility complex (MHC) molecules is the single most selective step in the recognition of pathogens by the cellular immune system. The human MHC genomic region (called HLA) is extremely polymorphic comprising several thousand alleles, each encoding a distinct MHC molecule. The potentially unique specificity of the majority of HLA alleles that have been identified to date remains uncharacterized. Likewise, only a limited number of chimpanzee and rhesus macaque MHC class I molecules have been characterized experimentally. Here, we present NetMHCpan-2.0, a method that generates quantitative predictions of the affinity of any peptide–MHC class I interaction. NetMHCpan-2.0 has been trained on the hitherto largest set of quantitative MHC binding data available, covering HLA-A and HLA-B, as well as chimpanzee, rhesus macaque, gorilla, and mouse MHC class I molecules. We show that the NetMHCpan-2.0 method can accurately predict binding to uncharacterized HLA molecules, including HLA-C and HLA-G. Moreover, NetMHCpan-2.0 is demonstrated to accurately predict peptide binding to chimpanzee and macaque MHC class I molecules. The power of NetMHCpan-2.0 to guide immunologists in interpreting cellular immune responses in large out-bred populations is demonstrated. Further, we used NetMHCpan-2.0 to predict potential binding peptides for the pig MHC class I molecule SLA-1*0401. Ninety-three percent of the predicted peptides were demonstrated to bind stronger than 500 nM. The high performance of NetMHCpan-2.0 for non-human primates documents the method’s ability to provide broad allelic coverage also beyond human MHC molecules. The method is available at http://www.cbs.dtu.dk/services/NetMHCpan . read more read less

Topics:

MHC class I (67%)67% related to the paper, Human leukocyte antigen (58%)58% related to the paper, CD74 (57%)57% related to the paper, Peptide binding (56%)56% related to the paper, Major histocompatibility complex (56%)56% related to the paper
View PDF
699 Citations
Journal Article DOI: 10.1007/BF00172176
Human T-cell receptor variable gene segment families.
Bernhard Arden1, Stephen P. Clark2, Dieter Kabelitz1, Tak W. Mak3
01 Jan 1995 - Immunogenetics

Abstract:

Multiple DNA and protein sequence alignments have been constructed for the human T-cell receptor alpha/delta, beta, and gamma (TCRA/D, B, and G) variable (V) gene segments. The traditional classification into subfamilies was confirmed using a much larger pool of sequences. For each sequence, a name was derived which complies ... Multiple DNA and protein sequence alignments have been constructed for the human T-cell receptor alpha/delta, beta, and gamma (TCRA/D, B, and G) variable (V) gene segments. The traditional classification into subfamilies was confirmed using a much larger pool of sequences. For each sequence, a name was derived which complies with the standard nomenclature. The traditional numbering of V gene segments in the order of their discovery was continued and changed when in conflict with names of other segments. By discriminating between alleles at the same locus versus genes from different loci, we were able to reduce the number of more than 150 different TCRBV sequences in the database to a repertoire of only 47 functional TCRBV gene segments. An extension of this analysis to the over 100 TCRAV sequences results in a predicted repertoire of 42 functional TCRAV gene segments. Our alignment revealed two residues that distinguish between the highly homologous V delta and V alpha, one at a site that in VH contacts the constant region, the other at the interface between immunoglobulin VH and VL. This site may be responsible for restricted pairing between certain V delta and V gamma chains. On the other hand, V beta and V gamma appear to be related by the fact that their CDR2 length is increased by four residues as compared with that of V alpha/delta peptides. read more read less

Topics:

Gene mutation (54%)54% related to the paper, Locus (genetics) (50%)50% related to the paper, Sequence alignment (50%)50% related to the paper
694 Citations
Journal Article DOI: 10.1007/S002510050594
Nine major HLA class I supertypes account for the vast preponderance of HLA-A and -B polymorphism.
01 Nov 1999 - Immunogenetics

Abstract:

Herein, we review the epitope approach to vaccine development, and discuss how knowledge of HLA supertypes might be used as a tool in the development of such vaccines. After reviewing the main structural features of the A2-, A3-, B7-, and B44- supertype alleles, and biological data demonstrating their immunological relevance,... Herein, we review the epitope approach to vaccine development, and discuss how knowledge of HLA supertypes might be used as a tool in the development of such vaccines. After reviewing the main structural features of the A2-, A3-, B7-, and B44- supertype alleles, and biological data demonstrating their immunological relevance, we analyze the frequency at which these supertype alleles are expressed in various ethnicities and discuss the relevance of those observations to vaccine development. Next, the existence of five new supertypes (A1, A24, B27, B58, and B62) is reported. As a result, it is possible to account for the predominance of all known HLA class I with only nine main functional binding specificities. The practical implications of this finding, as well as its relevance to understanding the functional implication of MHC polymorphism in humans, are discussed. read more read less

Topics:

Human leukocyte antigen (52%)52% related to the paper, HLA-A (51%)51% related to the paper
View PDF
633 Citations
Author Pic

SciSpace is a very innovative solution to the formatting problem and existing providers, such as Mendeley or Word did not really evolve in recent years.

- Andreas Frutiger, Researcher, ETH Zurich, Institute for Biomedical Engineering

Get MS-Word and LaTeX output to any Journal within seconds
1
Choose a template
Select a template from a library of 40,000+ templates
2
Import a MS-Word file or start fresh
It takes only few seconds to import
3
View and edit your final output
SciSpace will automatically format your output to meet journal guidelines
4
Submit directly or Download
Submit to journal directly or Download in PDF, MS Word or LaTeX

(Before submission check for plagiarism via Turnitin)

clock Less than 3 minutes

What to expect from SciSpace?

Speed and accuracy over MS Word

''

With SciSpace, you do not need a word template for Immunogenetics.

It automatically formats your research paper to Springer formatting guidelines and citation style.

You can download a submission ready research paper in pdf, LaTeX and docx formats.

Time comparison

Time taken to format a paper and Compliance with guidelines

Plagiarism Reports via Turnitin

SciSpace has partnered with Turnitin, the leading provider of Plagiarism Check software.

Using this service, researchers can compare submissions against more than 170 million scholarly articles, a database of 70+ billion current and archived web pages. How Turnitin Integration works?

Turnitin Stats
Publisher Logos

Freedom from formatting guidelines

One editor, 100K journal formats – world's largest collection of journal templates

With such a huge verified library, what you need is already there.

publisher-logos

Easy support from all your favorite tools

Immunogenetics format uses SPBASIC citation style.

Automatically format and order your citations and bibliography in a click.

SciSpace allows imports from all reference managers like Mendeley, Zotero, Endnote, Google Scholar etc.

Frequently asked questions

1. Can I write Immunogenetics in LaTeX?

Absolutely not! Our tool has been designed to help you focus on writing. You can write your entire paper as per the Immunogenetics guidelines and auto format it.

2. Do you follow the Immunogenetics guidelines?

Yes, the template is compliant with the Immunogenetics guidelines. Our experts at SciSpace ensure that. If there are any changes to the journal's guidelines, we'll change our algorithm accordingly.

3. Can I cite my article in multiple styles in Immunogenetics?

Of course! We support all the top citation styles, such as APA style, MLA style, Vancouver style, Harvard style, and Chicago style. For example, when you write your paper and hit autoformat, our system will automatically update your article as per the Immunogenetics citation style.

4. Can I use the Immunogenetics templates for free?

Sign up for our free trial, and you'll be able to use all our features for seven days. You'll see how helpful they are and how inexpensive they are compared to other options, Especially for Immunogenetics.

5. Can I use a manuscript in Immunogenetics that I have written in MS Word?

Yes. You can choose the right template, copy-paste the contents from the word document, and click on auto-format. Once you're done, you'll have a publish-ready paper Immunogenetics that you can download at the end.

6. How long does it usually take you to format my papers in Immunogenetics?

It only takes a matter of seconds to edit your manuscript. Besides that, our intuitive editor saves you from writing and formatting it in Immunogenetics.

7. Where can I find the template for the Immunogenetics?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Immunogenetics's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

8. Can I reformat my paper to fit the Immunogenetics's guidelines?

Of course! You can do this using our intuitive editor. It's very easy. If you need help, our support team is always ready to assist you.

9. Immunogenetics an online tool or is there a desktop version?

SciSpace's Immunogenetics is currently available as an online tool. We're developing a desktop version, too. You can request (or upvote) any features that you think would be helpful for you and other researchers in the "feature request" section of your account once you've signed up with us.

10. I cannot find my template in your gallery. Can you create it for me like Immunogenetics?

Sure. You can request any template and we'll have it setup within a few days. You can find the request box in Journal Gallery on the right side bar under the heading, "Couldn't find the format you were looking for like Immunogenetics?”

11. What is the output that I would get after using Immunogenetics?

After writing your paper autoformatting in Immunogenetics, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Immunogenetics's impact factor high enough that I should try publishing my article there?

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 these factors include review board, rejection rates, frequency of inclusion in indexes, and Eigenfactor. You need to assess all these factors before you make your final call.

13. What is Sherpa RoMEO Archiving Policy for Immunogenetics?

SHERPA/RoMEO Database

We extracted this data from Sherpa Romeo to help researchers understand the access level of this journal in accordance with the Sherpa Romeo Archiving Policy for Immunogenetics. The table below indicates the level of access a journal has as per Sherpa Romeo's 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.

14. What are the most common citation types In Immunogenetics?

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

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

15. How do I submit my article to the Immunogenetics?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Immunogenetics's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Immunogenetics in Endnote format?

Yes, SciSpace provides this functionality. After signing up, you would need to import your existing references from Word or Bib file to SciSpace. Then SciSpace would allow you to download your references in Immunogenetics Endnote style according to Elsevier guidelines.

Fast and reliable,
built for complaince.

Instant formatting to 100% publisher guidelines on - SciSpace.

Available only on desktops 🖥

No word template required

Typset automatically formats your research paper to Immunogenetics formatting guidelines and citation style.

Verifed journal formats

One editor, 100K journal formats.
With the largest collection of verified journal formats, what you need is already there.

Trusted by academicians

I spent hours with MS word for reformatting. It was frustrating - plain and simple. With SciSpace, I can draft my manuscripts and once it is finished I can just submit. In case, I have to submit to another journal it is really just a button click instead of an afternoon of reformatting.

Andreas Frutiger
Researcher & Ex MS Word user
Use this template