Example of Chromosoma format
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Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format Example of Chromosoma format
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This content is only for preview purposes. The original open access content can be found here.
open access Open Access

Chromosoma — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Genetics #54 of 325 up up by 15 ranks
Genetics (clinical) #15 of 87 up up by 7 ranks
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 153 Published Papers | 1176 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 04/07/2020
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SJR: 3.587
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open access Open Access

Springer

Quality:  
High
CiteRatio: 4.2
SJR: 0.966
SNIP: 1.086

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.

3.442

2% from 2018

Impact factor for Chromosoma from 2016 - 2019
Year Value
2019 3.442
2018 3.53
2017 4.021
2016 4.414
graph view Graph view
table view Table view

7.7

3% from 2019

CiteRatio for Chromosoma from 2016 - 2020
Year Value
2020 7.7
2019 7.9
2018 7.2
2017 7.1
2016 7.5
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.

insights Insights

  • CiteRatio of this journal has decreased by 3% 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.

1.945

20% from 2019

SJR for Chromosoma from 2016 - 2020
Year Value
2020 1.945
2019 2.425
2018 2.054
2017 2.678
2016 3.309
graph view Graph view
table view Table view

0.996

5% from 2019

SNIP for Chromosoma from 2016 - 2020
Year Value
2020 0.996
2019 1.052
2018 0.955
2017 1.045
2016 1.083
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has decreased by 20% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

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

Chromosoma

Guideline source: View

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Springer

Chromosoma

Chromosoma publishes research and review articles on the functional organization of the eukaryotic cell nucleus, with a particular emphasis on - the structure and dynamics of chromatin and chromosomes - the expression and replication of genomes - genome organization and evolut...... Read More

Genetics

Genetics(clinical)

Biochemistry, Genetics and Molecular Biology

i
Last updated on
04 Jul 2020
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ISSN
0009-5915
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Impact Factor
Medium - 0.756
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/BF00291041
A non-radioactive in situ hybridization method for the localization of specific RNAs in Drosophila embryos reveals translational control of the segmentation gene hunchback.
Diethard Tautz1, Christine Pfeifle1
01 Aug 1989 - Chromosoma

Abstract:

We have developed a non-radioactive in situ hybridization technique for the localization of RNA in whole mount Drosophila embryos. After fixation, whole embryos are hybridized in situ with a DNA probe which has been labeled with digoxygenin. The hybridization products are detected by using a phosphatase-coupled antibody again... We have developed a non-radioactive in situ hybridization technique for the localization of RNA in whole mount Drosophila embryos. After fixation, whole embryos are hybridized in situ with a DNA probe which has been labeled with digoxygenin. The hybridization products are detected by using a phosphatase-coupled antibody against digoxygenin. In parallel experiments, embryos can be treated with an antibody directed against the corresponding protein product to allow the detection of its distribution using standard immunochemical techniques. We have used this approach to compare the spatial and temporal distribution patterns of the RNA and protein products of the segmentation gene hunchback (hb) during the early stages of embryogenesis. This comparison revealed translational control of the maternally derived hb mRNA, which was difficult to detect by conventional techniques. The non-radioactive in situ hybridization method is as sensitive as conventional methods, but is faster and easier to perform. This may make it a useful tool for a variety of other systems. read more read less

Topics:

Hybridization probe (57%)57% related to the paper, In situ hybridization (53%)53% related to the paper, Drosophila embryogenesis (52%)52% related to the paper, Molecular probe (52%)52% related to the paper, Segmentation gene (51%)51% related to the paper
View PDF
2,327 Citations
Journal Article DOI: 10.1007/S004120050256
Mitosis-specific phosphorylation of histone H3 initiates primarily within pericentromeric heterochromatin during G2 and spreads in an ordered fashion coincident with mitotic chromosome condensation.
01 Nov 1997 - Chromosoma

Abstract:

We have generated and characterized a novel site-specific antibody highly specific for the phosphorylated form of the amino-terminus of histone H3 (Ser10). In this study, we used this antibody to examine in detail the relationship between H3 phosphorylation and mitotic chromosome condensation in mammalian cells. Our results e... We have generated and characterized a novel site-specific antibody highly specific for the phosphorylated form of the amino-terminus of histone H3 (Ser10). In this study, we used this antibody to examine in detail the relationship between H3 phosphorylation and mitotic chromosome condensation in mammalian cells. Our results extend previous biochemical studies by demonstrating that mitotic phosphorylation of H3 initiates nonrandomly in pericentromeric heterochromatin in late G2 interphase cells. Following initiation, H3 phosphorylation appears to spread throughout the condensing chromatin and is complete in most cell lines just prior to the formation of prophase chromosomes, in which a phosphorylated, but nonmitotic, chromosomal organization is observed. In general, there is a precise spatial and temporal correlation between H3 phosphorylation and initial stages of chromatin condensation. Dephosphorylation of H3 begins in anaphase and is complete immediately prior to detectable chromosome decondensation in telophase cells. We propose that the singular phosphorylation of the amino-terminus of histone H3 may be involved in facilitating two key functions during mitosis: (1) regulate protein-protein interactions to promote binding of trans-acting factors that "drive" chromatin condensation as cells enter M-phase and (2) coordinate chromatin decondensation associated with M-phase. read more read less

Topics:

Mitotic chromosome condensation (71%)71% related to the paper, Premature chromosome condensation (67%)67% related to the paper, Chromosome decondensation (63%)63% related to the paper, Prophase (61%)61% related to the paper, Chromatin (61%)61% related to the paper
1,852 Citations
Journal Article DOI: 10.1007/BF00329389
Visualization of nucleolar organizer regions im mammalian chromosomes using silver staining
Carll Goodpasture1, Stephen E. Bloom1
20 Nov 1975 - Chromosoma

Abstract:

A simple ammoniacal silver staining procedure, designated Ag-AS, differentially stains the chromosomal locations of ribosomal DNA in certain mammalian species. This was critically demonstrated by Ag-AS staining of the nucleolus organizer regions in karyotypes of the same species and cell lines used for locating the ribosomal ... A simple ammoniacal silver staining procedure, designated Ag-AS, differentially stains the chromosomal locations of ribosomal DNA in certain mammalian species. This was critically demonstrated by Ag-AS staining of the nucleolus organizer regions in karyotypes of the same species and cell lines used for locating the ribosomal cistrons by DNA/RNA in situ hybridization. With Ag-AS, silver stained NORs (Ag-NORs) are visualized as black spherical bodies on yellow-brown chromosome arms. Ag-NORs were visualized throughout mitosis at the secondary constrictions in the rat kangaroo, Seba's fruit bat, Indian muntjac, and Rhesus monkey. The Chinese hamster and cattle have telomeric Ag-NORs, the mouse subcentromeric Ag-NORs, and the field vole Ag-NORs as minute short arms or choromosomal satellites. Ag-NORs occur at both secondary constrictions and at telomeres in the cotton rat. Variability in Ag-NOR pattern included differences in the number of Ag-NORs per cell within a cell population, size of Ag-NORs among chromosomes of a complement, and presence of Ag-NOR on particular chromosomes in two cell lines of the Chinese hamster. The available cytochemical data suggest that the Ag-AS reaction stains chromosomal proteins at the NOR rather than the rDNA itself. read more read less

Topics:

Nucleolus organizer region (62%)62% related to the paper, Nucleolar Organizer Region (59%)59% related to the paper, Ribosomal DNA (57%)57% related to the paper, Field vole (55%)55% related to the paper, Silver Staining Method (54%)54% related to the paper
1,082 Citations
Journal Article DOI: 10.1007/BF00282002
Identification of human chromosomes by DNA-binding fluorescent agents
01 Jan 1970 - Chromosoma

Abstract:

The distribution of DNA along metaphase chromosomes that are not excessively contracted can be visualized in the fluorescence microscope with the aid of fluorescent DNA-binding agents. Additional, characteristic details in the fluorescence patterns are obtained with fluorochromes that bind preferentially to certain chromosoma... The distribution of DNA along metaphase chromosomes that are not excessively contracted can be visualized in the fluorescence microscope with the aid of fluorescent DNA-binding agents. Additional, characteristic details in the fluorescence patterns are obtained with fluorochromes that bind preferentially to certain chromosomal regions. The highly fluorescent alkylating agent quinacrine mustard (QM) effects discrete, fluorescent labeling of both plant and mammalian metaphase chromosomes, presumably by selective binding to guanine residues in DNA, and is also capable of intercalation in the DNA double helix. Chromosome regions fluorescing particularly strongly with QM have been demonstrated in human metaphase chromosomes 3, 13–15 and Y. A convenient measuring technique has been developed for the rapid and accurate recording of fluorescence patterns in human metaphase chromosomes. These photoelectric recordings of the fluorescence patterns contain far greater detail than can be seen by the human eye. The fluorescence patterns described are based on measurements of about 1,000 human metaphase chromosomes. This new technique of determining fluorescence patterns in human chromosomes should be particularly valuable for the identification of chromosomes 4–5 and the individual types in the 6–12 group. Individual, typical patterns also occur within the groups 13–15, 17–18, and 21–22. read more read less

Topics:

Metaphase (61%)61% related to the paper, Fluorescence microscope (53%)53% related to the paper, Quinacrine Mustard (51%)51% related to the paper
919 Citations
Journal Article DOI: 10.1007/BF00292840
Reverse fluorescent chromosome banding with chromomycin and DAPI.
29 Nov 1976 - Chromosoma

Abstract:

Two DNA binding guanine-specific antibiotics, chromomycin A3 (CMA) and the closely related mithramycin (MM), were used as chromosome fluorescent dyes. Root-tip metaphase chromosomes of three plant species and human metaphase chromosomes were sequentially stained with CMA or MM and the DNA binding AT-specific fluorochrome 4'-6... Two DNA binding guanine-specific antibiotics, chromomycin A3 (CMA) and the closely related mithramycin (MM), were used as chromosome fluorescent dyes. Root-tip metaphase chromosomes of three plant species and human metaphase chromosomes were sequentially stained with CMA or MM and the DNA binding AT-specific fluorochrome 4'-6-diamidino-2-phenylindole (DAPI). In some cases a non-fluorescent counterstain was used as contrasting agent: methyl green in conjunction with CMA, and actinomycin D (AMD) in combination with DAPI.--In all three plant species, Vicia faba, Scilla siberica, and Ornithogalum caudatum, the nucleolus organiser regions and/or associated heterochromatin displayed very bright fluorescence with CMA and MM and, in general, heterochromatic segments (C-bands) which were bright with CMA and MM were pale with DAPI whereas segments which were dim with CMA and MM displayed very bright fluorescence with DAPI.--Human metaphase chromosomes showed a small longitudinal differentiation in CMA fluorescence, which was essentially the reverse of the banding pattern obtained with AMD/DAPI double-staining, but of lower contrast. The cma-banding pattern appears to be similar to the pattern found by R-banding procedures. read more read less

Topics:

Chromomycin A3 (53%)53% related to the paper, Metaphase (51%)51% related to the paper, DAPI (50%)50% related to the paper
908 Citations
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With SciSpace, you do not need a word template for Chromosoma.

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Chromosoma format uses SPBASIC citation style.

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Frequently asked questions

1. Can I write Chromosoma in LaTeX?

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

2. Do you follow the Chromosoma guidelines?

Yes, the template is compliant with the Chromosoma 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 Chromosoma?

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 Chromosoma citation style.

4. Can I use the Chromosoma 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 Chromosoma.

5. Can I use a manuscript in Chromosoma 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 Chromosoma that you can download at the end.

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

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

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

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 Chromosoma'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 Chromosoma'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. Chromosoma an online tool or is there a desktop version?

SciSpace's Chromosoma 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 Chromosoma?

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 Chromosoma?”

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

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

12. Is Chromosoma'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 Chromosoma?

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 Chromosoma. 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 Chromosoma?

The 5 most common citation types in order of usage for Chromosoma 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 Chromosoma?

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 Chromosoma's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Chromosoma 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 Chromosoma Endnote style according to Elsevier guidelines.

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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.

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