Journal article 46104 views 127 downloads
Clinical Functional Genomics
Cancers, Volume: 13, Issue: 18, Start page: 4627
Swansea University Author: Steve Conlan
-
PDF | Version of Record
© 2021 by the authors. This is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license
Download (1.11MB)
DOI (Published version): 10.3390/cancers13184627
Abstract
Functional genomics is the study of how the genome and its products, including RNA and proteins, function and interact to affect different biological processes. The field of functional genomics includes transcriptomics, proteomics, metabolomics and epigenomics, as these all relate to controlling the...
Published in: | Cancers |
---|---|
ISSN: | 2072-6694 |
Published: |
MDPI AG
2021
|
Online Access: |
Check full text
|
URI: | https://cronfa.swan.ac.uk/Record/cronfa57903 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
first_indexed |
2021-09-28T16:42:39Z |
---|---|
last_indexed |
2021-09-29T03:22:14Z |
id |
cronfa57903 |
recordtype |
SURis |
fullrecord |
<?xml version="1.0"?><rfc1807><datestamp>2021-09-28T17:48:28.9177743</datestamp><bib-version>v2</bib-version><id>57903</id><entry>2021-09-16</entry><title>Clinical Functional Genomics</title><swanseaauthors><author><sid>0bb6bd247e32fb4249de62c0013b51cb</sid><ORCID>0000-0002-2562-3461</ORCID><firstname>Steve</firstname><surname>Conlan</surname><name>Steve Conlan</name><active>true</active><ethesisStudent>false</ethesisStudent></author></swanseaauthors><date>2021-09-16</date><deptcode>BMS</deptcode><abstract>Functional genomics is the study of how the genome and its products, including RNA and proteins, function and interact to affect different biological processes. The field of functional genomics includes transcriptomics, proteomics, metabolomics and epigenomics, as these all relate to controlling the genome leading to expression of particular phenotypes. By studying whole genomes—clinical genomics, transcriptomes and epigenomes—functional genomics allows the exploration of the diverse relationship between genotype and phenotype, not only for humans as a species but also in individuals, allowing an understanding and evaluation of how the functional genome ‘contributes’ to different diseases. Functional variation in disease can help us better understand that disease, although it is currently limited in terms of ethnic diversity, and will ultimately give way to more personalized treatment plans.</abstract><type>Journal Article</type><journal>Cancers</journal><volume>13</volume><journalNumber>18</journalNumber><paginationStart>4627</paginationStart><paginationEnd/><publisher>MDPI AG</publisher><placeOfPublication/><isbnPrint/><isbnElectronic/><issnPrint/><issnElectronic>2072-6694</issnElectronic><keywords>functional genomics; clinical adoption; CRISPR; single cell analysis; ethnic diversity</keywords><publishedDay>15</publishedDay><publishedMonth>9</publishedMonth><publishedYear>2021</publishedYear><publishedDate>2021-09-15</publishedDate><doi>10.3390/cancers13184627</doi><url/><notes/><college>COLLEGE NANME</college><department>Biomedical Sciences</department><CollegeCode>COLLEGE CODE</CollegeCode><DepartmentCode>BMS</DepartmentCode><institution>Swansea University</institution><apcterm/><funders>This research was funded by the Swansea University Employability Academy Internship Programme 2021 (S.C.)</funders><lastEdited>2021-09-28T17:48:28.9177743</lastEdited><Created>2021-09-16T07:50:03.2665560</Created><path><level id="1">Faculty of Medicine, Health and Life Sciences</level><level id="2">Swansea University Medical School - Medicine</level></path><authors><author><firstname>Seren</firstname><surname>Carpenter</surname><order>1</order></author><author><firstname>Steve</firstname><surname>Conlan</surname><orcid>0000-0002-2562-3461</orcid><order>2</order></author></authors><documents><document><filename>57903__21044__0c09a9e74db5494e99bc09b560d833b0.pdf</filename><originalFilename>57903.pdf</originalFilename><uploaded>2021-09-28T17:46:09.6584710</uploaded><type>Output</type><contentLength>1166767</contentLength><contentType>application/pdf</contentType><version>Version of Record</version><cronfaStatus>true</cronfaStatus><documentNotes>© 2021 by the authors. This is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license</documentNotes><copyrightCorrect>true</copyrightCorrect><language>eng</language><licence>https://creativecommons.org/licenses/by/4.0/</licence></document></documents><OutputDurs/></rfc1807> |
spelling |
2021-09-28T17:48:28.9177743 v2 57903 2021-09-16 Clinical Functional Genomics 0bb6bd247e32fb4249de62c0013b51cb 0000-0002-2562-3461 Steve Conlan Steve Conlan true false 2021-09-16 BMS Functional genomics is the study of how the genome and its products, including RNA and proteins, function and interact to affect different biological processes. The field of functional genomics includes transcriptomics, proteomics, metabolomics and epigenomics, as these all relate to controlling the genome leading to expression of particular phenotypes. By studying whole genomes—clinical genomics, transcriptomes and epigenomes—functional genomics allows the exploration of the diverse relationship between genotype and phenotype, not only for humans as a species but also in individuals, allowing an understanding and evaluation of how the functional genome ‘contributes’ to different diseases. Functional variation in disease can help us better understand that disease, although it is currently limited in terms of ethnic diversity, and will ultimately give way to more personalized treatment plans. Journal Article Cancers 13 18 4627 MDPI AG 2072-6694 functional genomics; clinical adoption; CRISPR; single cell analysis; ethnic diversity 15 9 2021 2021-09-15 10.3390/cancers13184627 COLLEGE NANME Biomedical Sciences COLLEGE CODE BMS Swansea University This research was funded by the Swansea University Employability Academy Internship Programme 2021 (S.C.) 2021-09-28T17:48:28.9177743 2021-09-16T07:50:03.2665560 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Seren Carpenter 1 Steve Conlan 0000-0002-2562-3461 2 57903__21044__0c09a9e74db5494e99bc09b560d833b0.pdf 57903.pdf 2021-09-28T17:46:09.6584710 Output 1166767 application/pdf Version of Record true © 2021 by the authors. This is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license true eng https://creativecommons.org/licenses/by/4.0/ |
title |
Clinical Functional Genomics |
spellingShingle |
Clinical Functional Genomics Steve Conlan |
title_short |
Clinical Functional Genomics |
title_full |
Clinical Functional Genomics |
title_fullStr |
Clinical Functional Genomics |
title_full_unstemmed |
Clinical Functional Genomics |
title_sort |
Clinical Functional Genomics |
author_id_str_mv |
0bb6bd247e32fb4249de62c0013b51cb |
author_id_fullname_str_mv |
0bb6bd247e32fb4249de62c0013b51cb_***_Steve Conlan |
author |
Steve Conlan |
author2 |
Seren Carpenter Steve Conlan |
format |
Journal article |
container_title |
Cancers |
container_volume |
13 |
container_issue |
18 |
container_start_page |
4627 |
publishDate |
2021 |
institution |
Swansea University |
issn |
2072-6694 |
doi_str_mv |
10.3390/cancers13184627 |
publisher |
MDPI AG |
college_str |
Faculty of Medicine, Health and Life Sciences |
hierarchytype |
|
hierarchy_top_id |
facultyofmedicinehealthandlifesciences |
hierarchy_top_title |
Faculty of Medicine, Health and Life Sciences |
hierarchy_parent_id |
facultyofmedicinehealthandlifesciences |
hierarchy_parent_title |
Faculty of Medicine, Health and Life Sciences |
department_str |
Swansea University Medical School - Medicine{{{_:::_}}}Faculty of Medicine, Health and Life Sciences{{{_:::_}}}Swansea University Medical School - Medicine |
document_store_str |
1 |
active_str |
0 |
description |
Functional genomics is the study of how the genome and its products, including RNA and proteins, function and interact to affect different biological processes. The field of functional genomics includes transcriptomics, proteomics, metabolomics and epigenomics, as these all relate to controlling the genome leading to expression of particular phenotypes. By studying whole genomes—clinical genomics, transcriptomes and epigenomes—functional genomics allows the exploration of the diverse relationship between genotype and phenotype, not only for humans as a species but also in individuals, allowing an understanding and evaluation of how the functional genome ‘contributes’ to different diseases. Functional variation in disease can help us better understand that disease, although it is currently limited in terms of ethnic diversity, and will ultimately give way to more personalized treatment plans. |
published_date |
2021-09-15T04:13:59Z |
_version_ |
1763753946673840128 |
score |
11.03559 |