Example of Frontiers in Bioengineering and Biotechnology format
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Example of Frontiers in Bioengineering and Biotechnology format Example of Frontiers in Bioengineering and Biotechnology format Example of Frontiers in Bioengineering and Biotechnology format Example of Frontiers in Bioengineering and Biotechnology format Example of Frontiers in Bioengineering and Biotechnology format Example of Frontiers in Bioengineering and Biotechnology format Example of Frontiers in Bioengineering and Biotechnology format Example of Frontiers in Bioengineering and Biotechnology format Example of Frontiers in Bioengineering and Biotechnology format Example of Frontiers in Bioengineering and Biotechnology format Example of Frontiers in Bioengineering and Biotechnology format Example of Frontiers in Bioengineering and Biotechnology format Example of Frontiers in Bioengineering and Biotechnology format Example of Frontiers in Bioengineering and Biotechnology format Example of Frontiers in Bioengineering and Biotechnology format
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open access Open Access

Frontiers in Bioengineering and Biotechnology — Template for authors

Publisher: Frontiers Media
Categories Rank Trend in last 3 yrs
Histology #34 of 60 down down by 25 ranks
Biotechnology #158 of 282 down down by 113 ranks
Biomedical Engineering #131 of 229 down down by 91 ranks
Bioengineering #97 of 148 down down by 65 ranks
journal-quality-icon Journal quality:
Medium
calendar-icon Last 4 years overview: 2081 Published Papers | 5831 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 08/07/2020
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Related Journals

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Quality:  
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SJR: 1.279
SNIP: 0.942
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CiteRatio: 13.9
SJR: 2.328
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Nature

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Quality:  
High
CiteRatio: 37.4
SJR: 15.358
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Journal Performance & Insights

CiteRatio

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

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

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.

2.8

13% from 2019

CiteRatio for Frontiers in Bioengineering and Biotechnology from 2016 - 2020
Year Value
2020 2.8
2019 3.2
2018 6.1
2017 6.4
graph view Graph view
table view Table view

1.081

19% from 2019

SJR for Frontiers in Bioengineering and Biotechnology from 2017 - 2020
Year Value
2020 1.081
2019 0.908
2018 1.248
2017 1.565
graph view Graph view
table view Table view

1.339

17% from 2019

SNIP for Frontiers in Bioengineering and Biotechnology from 2017 - 2020
Year Value
2020 1.339
2019 1.149
2018 1.327
2017 1.043
graph view Graph view
table view Table view

insights Insights

  • CiteRatio of this journal has decreased by 13% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

insights Insights

  • SJR of this journal has increased by 19% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 17% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Frontiers in Bioengineering and Biotechnology

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Frontiers Media

Frontiers in Bioengineering and Biotechnology

Approved by publishing and review experts on SciSpace, this template is built as per for Frontiers in Bioengineering and Biotechnology formatting guidelines as mentioned in Frontiers Media author instructions. The current version was created on 08 Jul 2020 and has been used by 486 authors to write and format their manuscripts to this journal.

Medicine

i
Last updated on
08 Jul 2020
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ISSN
2296-4185
i
Open Access
No
i
Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
i
Endnote Style
Download Available
i
Bibliography Name
frontiersinSCNS_ENG_HUMS
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Citation Type
Numbered
[25]
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Bibliography Example
Blonder GE, Tinkham M, Klapwijk TM. Transition from metallic to tunneling regimes in superconducting microconstrictions: Excess current, charge imbalance, and supercurrent conversion. Phys. Rev. B 25 (1982) 4515–4532.

Top papers written in this journal

open accessOpen access Journal Article DOI: 10.3389/FBIOE.2016.00012
In Vitro Tumor Models: Advantages, Disadvantages, Variables, and Selecting the Right Platform
Moriah E. Katt1, Amanda L. Placone1, Andrew D. Wong1, Zinnia S. Xu1, Peter C. Searson1

Abstract:

In vitro tumor models have provided important tools for cancer research and serve as low-cost screening platforms for drug therapies; however, cancer recurrence remains largely unchecked due to metastasis, which is the cause of the majority of cancer related deaths. The need for an improved understanding of the progression an... In vitro tumor models have provided important tools for cancer research and serve as low-cost screening platforms for drug therapies; however, cancer recurrence remains largely unchecked due to metastasis, which is the cause of the majority of cancer related deaths. The need for an improved understanding of the progression and treatment of cancer has pushed for increased accuracy and physiological relevance of in vitro tumor models. As a result, in vitro tumor models have concurrently increased in complexity and their output parameters further diversified, since these models have progressed beyond simple proliferation, invasion, and cytotoxicity screens and have begun recapitulating critical steps in the metastatic cascade, such as intravasation, extravasation, angiogenesis, matrix remodeling, and tumor cell dormancy. Advances in tumor cell biology, 3D cell culture, tissue engineering, biomaterials, microfabrication, and microfluidics have enabled rapid development of new in vitro tumor models that often incorporate multiple cell types, extracellular matrix materials, and spatial and temporal introduction of soluble factors. Other innovations include the incorporation of perfusable microvessels to simulate the tumor vasculature and model intravasation and extravasation. The drive towards precision medicine has increased interest in adapting in vitro tumor models for patient-specific therapies, clinical management, and assessment of metastatic potential. Here, we review the wide range of current in vitro tumor models and summarize their advantages, disadvantages, and suitability in modeling specific aspects of the metastatic cascade and drug treatment. read more read less

Topics:

Tumor Cell Biology (61%)61% related to the paper, Intravasation (57%)57% related to the paper
View PDF
548 Citations
open accessOpen access Journal Article DOI: 10.3389/FBIOE.2015.00023
Analytical Methods in Untargeted Metabolomics: State of the Art in 2015
Arnald Alonso1, Sara Marsal, Antonio Julià

Abstract:

Metabolomics comprises the methods and techniques that are used to measure the small molecule composition of biofluids and tissues, and is actually one of the most rapidly evolving research fields. The determination of the metabolomic profile –the metabolome- has multiple applications in many biological sciences, including th... Metabolomics comprises the methods and techniques that are used to measure the small molecule composition of biofluids and tissues, and is actually one of the most rapidly evolving research fields. The determination of the metabolomic profile –the metabolome- has multiple applications in many biological sciences, including the developing of new diagnostic tools in medicine. Recent technological advances in nuclear magnetic resonance (NMR) and mass spectrometry (MS) are significantly improving our capacity to obtain more data from each biological sample. Consequently, there is a need for fast and accurate statistical and bioinformatic tools that can deal with the complexity and volume of the data generated in metabolomic studies. In this review we provide an update of the most commonly used analytical methods in metabolomics, starting from raw data processing and ending with pathway analysis and biomarker identification. Finally, the integration of metabolomic profiles with molecular data from other high throughput biotechnologies is also reviewed. read more read less

Topics:

Metabolomics (50%)50% related to the paper
View PDF
518 Citations
open accessOpen access Journal Article DOI: 10.3389/FBIOE.2020.00001
Cryopreservation of Human iPS Cell Aggregates in a DMSO-Free Solution-An Optimization and Comparative Study.
Rui Li1, Kathlyn Hornberger1, James R. Dutton1, Allison Hubel1

Abstract:

Human induced pluripotent stem cells (hiPSCs) are an important cell source for regenerative medicine products. Effective methods of preservation are critical to their clinical and commercial applications. The use of a dimethyl sulfoxide (DMSO)-free solution containing all non-toxic molecules offers an effective alternative to... Human induced pluripotent stem cells (hiPSCs) are an important cell source for regenerative medicine products. Effective methods of preservation are critical to their clinical and commercial applications. The use of a dimethyl sulfoxide (DMSO)-free solution containing all non-toxic molecules offers an effective alternative to the conventional DMSO and alleviates pain points associated with the use of DMSO in the cryopreservation of hiPSCs. Both hiPSCs and cells differentiated from them are commonly multicellular systems, which are more sensitive to stresses of freezing and thawing than single cells. In this investigation, low-temperature Raman spectroscopy visualized freezing behaviors of hiPSC aggregates in different solutions. These aggregates exhibited sensitivity to undercooling in DMSO-containing solutions. We demonstrated the ability to replace DMSO with non-toxic molecules, improve post-thaw cell survival, and reduce sensitivity to undercooling. An accelerated optimization process capitalized on the positive synergy among multiple DMSO-free molecules, which acted in concert to influence ice formation and protect cells during freezing and thawing. A differential evolution algorithm was used to optimize the multi-variable, DMSO-free preservation protocol in 8 experiments. hiPSC aggregates frozen in the optimized solution did not exhibit the same sensitivity to undercooling as those frozen in non-optimized solutions or DMSO, indicating superior adaptability of the optimized solution to different freezing modalities and unplanned deviations. This investigation shows the importance of optimization, explains the mechanisms and advantages of a DMSO-free solution, and enables not only improved cryopreservation of hiPSCs but potentially other cell types for translational regenerative medicine. read more read less
View PDF
477 Citations
open accessOpen access Journal Article DOI: 10.3389/FBIOE.2019.00001
Gene-Expressing Liposomes as Synthetic Cells for Molecular Communication Studies.
Giordano Rampioni1, Francesca D'Angelo1, Livia Leoni1, Pasquale Stano2

Abstract:

The bottom-up branch of synthetic biology includes-among others-innovative studies that combine cell-free protein synthesis with liposome technology to generate cell-like systems of minimal complexity, often referred to as synthetic cells. The functions of this type of synthetic cell derive from gene expression, hence they ca... The bottom-up branch of synthetic biology includes-among others-innovative studies that combine cell-free protein synthesis with liposome technology to generate cell-like systems of minimal complexity, often referred to as synthetic cells. The functions of this type of synthetic cell derive from gene expression, hence they can be programmed in a modular, progressive and customizable manner by means of ad hoc designed genetic circuits. This experimental scenario is rapidly expanding and synthetic cell research already counts numerous successes. Here, we present a review focused on the exchange of chemical signals between liposome-based synthetic cells (operating by gene expression) and biological cells, as well as between two populations of synthetic cells. The review includes a short presentation of the "molecular communication technologies," briefly discussing their promises and challenges. read more read less

Topics:

Synthetic biology (59%)59% related to the paper, Cell-free protein synthesis (51%)51% related to the paper
View PDF
433 Citations
open accessOpen access Journal Article DOI: 10.3389/FBIOE.2016.00004
Carbonate Precipitation through Microbial Activities in Natural Environment, and Their Potential in Biotechnology: A Review
Tingting Zhu1, Maria Dittrich1

Abstract:

Calcium carbonate represents a large portion of carbon reservoir and is used commercially for a variety of applications. Microbial carbonate precipitation (MCP), a by-product of microbial activities, plays an important metal coprecipitation and cementation role in natural systems. This natural process occurring in various geo... Calcium carbonate represents a large portion of carbon reservoir and is used commercially for a variety of applications. Microbial carbonate precipitation (MCP), a by-product of microbial activities, plays an important metal coprecipitation and cementation role in natural systems. This natural process occurring in various geological settings can be mimicked and used for a number of biotechnology such as metal remediation, carbon sequestration, enhanced oil recovery and construction restoration. In this study, different metabolic activities leading to calcium carbonate precipitation, their native environment, and potential applications and challenges are reviewed. read more read less

Topics:

Carbonate (57%)57% related to the paper, Calcium carbonate (53%)53% related to the paper, Carbon sequestration (50%)50% related to the paper
View PDF
415 Citations
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Frontiers in Bioengineering and Biotechnology format uses frontiersinSCNS_ENG_HUMS citation style.

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Frequently asked questions

1. Can I write Frontiers in Bioengineering and Biotechnology in LaTeX?

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

2. Do you follow the Frontiers in Bioengineering and Biotechnology guidelines?

Yes, the template is compliant with the Frontiers in Bioengineering and Biotechnology 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 Frontiers in Bioengineering and Biotechnology?

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 Frontiers in Bioengineering and Biotechnology citation style.

4. Can I use the Frontiers in Bioengineering and Biotechnology 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 Frontiers in Bioengineering and Biotechnology.

5. Can I use a manuscript in Frontiers in Bioengineering and Biotechnology 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 Frontiers in Bioengineering and Biotechnology that you can download at the end.

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

7. Where can I find the template for the Frontiers in Bioengineering and Biotechnology?

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

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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.

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SciSpace's Frontiers in Bioengineering and Biotechnology 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.

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

12. Is Frontiers in Bioengineering and Biotechnology'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 Frontiers in Bioengineering and Biotechnology?

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 Frontiers in Bioengineering and Biotechnology. 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 Frontiers in Bioengineering and Biotechnology?

The 5 most common citation types in order of usage for Frontiers in Bioengineering and Biotechnology 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 Frontiers in Bioengineering and Biotechnology?

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

16. Can I download Frontiers in Bioengineering and Biotechnology 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 Frontiers in Bioengineering and Biotechnology Endnote style according to Elsevier guidelines.

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