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HumCFS: a database of fragile sites in human chromosomes
BACKGROUND: Fragile sites are the chromosomal regions that are susceptible to breakage, and their frequency varies among the human population. Based on the frequency of fragile site induction, they are categorized as common and rare fragile sites. Common fragile sites are sensitive to replication st...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402404/ https://www.ncbi.nlm.nih.gov/pubmed/30999860 http://dx.doi.org/10.1186/s12864-018-5330-5 |
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author | Kumar, Rajesh Nagpal, Gandharva Kumar, Vinod Usmani, Salman Sadullah Agrawal, Piyush Raghava, Gajendra P. S. |
author_facet | Kumar, Rajesh Nagpal, Gandharva Kumar, Vinod Usmani, Salman Sadullah Agrawal, Piyush Raghava, Gajendra P. S. |
author_sort | Kumar, Rajesh |
collection | PubMed |
description | BACKGROUND: Fragile sites are the chromosomal regions that are susceptible to breakage, and their frequency varies among the human population. Based on the frequency of fragile site induction, they are categorized as common and rare fragile sites. Common fragile sites are sensitive to replication stress and often rearranged in cancer. Rare fragile sites are the archetypal trinucleotide repeats. Fragile sites are known to be involved in chromosomal rearrangements in tumors. Human miRNA genes are also present at fragile sites. A better understanding of genes and miRNAs lying in the fragile site regions and their association with disease progression is required. RESULT: HumCFS is a manually curated database of human chromosomal fragile sites. HumCFS provides useful information on fragile sites such as coordinates on the chromosome, cytoband, their chemical inducers and frequency of fragile site (rare or common), genes and miRNAs lying in fragile sites. Protein coding genes in the fragile sites were identified by mapping the coordinates of fragile sites with human genome Ensembl (GRCh38/hg38). Genes present in fragile sites were further mapped to DisGenNET database, to understand their possible link with human diseases. Human miRNAs from miRBase was also mapped on fragile site coordinates. In brief, HumCFS provides useful information about 125 human chromosomal fragile sites and their association with 4921 human protein-coding genes and 917 human miRNA’s. CONCLUSION: User-friendly web-interface of HumCFS and hyper-linking with other resources will help researchers to search for genes, miRNAs efficiently and to intersect the relationship among them. For easy data retrieval and analysis, we have integrated standard web-based tools, such as JBrowse, BLAST etc. Also, the user can download the data in various file formats such as text files, gff3 files and Bed-format files which can be used on UCSC browser. Database URL: http://webs.iiitd.edu.in/raghava/humcfs/ ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5330-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7402404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74024042020-08-07 HumCFS: a database of fragile sites in human chromosomes Kumar, Rajesh Nagpal, Gandharva Kumar, Vinod Usmani, Salman Sadullah Agrawal, Piyush Raghava, Gajendra P. S. BMC Genomics Database BACKGROUND: Fragile sites are the chromosomal regions that are susceptible to breakage, and their frequency varies among the human population. Based on the frequency of fragile site induction, they are categorized as common and rare fragile sites. Common fragile sites are sensitive to replication stress and often rearranged in cancer. Rare fragile sites are the archetypal trinucleotide repeats. Fragile sites are known to be involved in chromosomal rearrangements in tumors. Human miRNA genes are also present at fragile sites. A better understanding of genes and miRNAs lying in the fragile site regions and their association with disease progression is required. RESULT: HumCFS is a manually curated database of human chromosomal fragile sites. HumCFS provides useful information on fragile sites such as coordinates on the chromosome, cytoband, their chemical inducers and frequency of fragile site (rare or common), genes and miRNAs lying in fragile sites. Protein coding genes in the fragile sites were identified by mapping the coordinates of fragile sites with human genome Ensembl (GRCh38/hg38). Genes present in fragile sites were further mapped to DisGenNET database, to understand their possible link with human diseases. Human miRNAs from miRBase was also mapped on fragile site coordinates. In brief, HumCFS provides useful information about 125 human chromosomal fragile sites and their association with 4921 human protein-coding genes and 917 human miRNA’s. CONCLUSION: User-friendly web-interface of HumCFS and hyper-linking with other resources will help researchers to search for genes, miRNAs efficiently and to intersect the relationship among them. For easy data retrieval and analysis, we have integrated standard web-based tools, such as JBrowse, BLAST etc. Also, the user can download the data in various file formats such as text files, gff3 files and Bed-format files which can be used on UCSC browser. Database URL: http://webs.iiitd.edu.in/raghava/humcfs/ ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5330-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-18 /pmc/articles/PMC7402404/ /pubmed/30999860 http://dx.doi.org/10.1186/s12864-018-5330-5 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Database Kumar, Rajesh Nagpal, Gandharva Kumar, Vinod Usmani, Salman Sadullah Agrawal, Piyush Raghava, Gajendra P. S. HumCFS: a database of fragile sites in human chromosomes |
title | HumCFS: a database of fragile sites in human chromosomes |
title_full | HumCFS: a database of fragile sites in human chromosomes |
title_fullStr | HumCFS: a database of fragile sites in human chromosomes |
title_full_unstemmed | HumCFS: a database of fragile sites in human chromosomes |
title_short | HumCFS: a database of fragile sites in human chromosomes |
title_sort | humcfs: a database of fragile sites in human chromosomes |
topic | Database |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402404/ https://www.ncbi.nlm.nih.gov/pubmed/30999860 http://dx.doi.org/10.1186/s12864-018-5330-5 |
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