Current Challenges in Bioinformatics of Single Cell Genomics
Single cell genomics is a rapidly growing field with many new techniques emerging in the past few years. However, few bioinformatics tools specific for single cell genomics analysis are available. Single cell DNA/RNA sequencing data usually have low genome coverage and high amplification bias, which...
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doaj-d155876d2aa84fc8aead0bec83a66b7b2020-11-24T21:05:33ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2014-01-01410.3389/fonc.2014.0000773667Current Challenges in Bioinformatics of Single Cell GenomicsLuwen eNing0Geng eLiu1Guibo eLi2Yong eHou3Yin eTong4Jiankui eHe5South University of Science and Technology of ChinaBGI-ShenzhenBGI-ShenzhenBGI-ShenzhenSouth University of Science and Technology of ChinaSouth University of Science and Technology of ChinaSingle cell genomics is a rapidly growing field with many new techniques emerging in the past few years. However, few bioinformatics tools specific for single cell genomics analysis are available. Single cell DNA/RNA sequencing data usually have low genome coverage and high amplification bias, which makes bioinformatics analysis challenging. Many current bioinformatics tools developed for bulk cell sequencing do not work well with single cell sequencing data. Here, we summarize current challenges in the bioinformatics analysis of single cell genomic DNA sequencing and single cell transcriptomes. These challenges include calling copy number variations, identifying mutated genes in tumor samples, reconstructing cell lineages, recovering low abundant transcripts, and improving the accuracy of quantitative analysis of transcripts. Development in single cell genomics bioinformatics analysis will promote the application of this technology to basic biology and medical research.http://journal.frontiersin.org/Journal/10.3389/fonc.2014.00007/fullSNPDNA SEQUENCINGCNVsingle cell analysisRNA sequencing |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Luwen eNing Geng eLiu Guibo eLi Yong eHou Yin eTong Jiankui eHe |
spellingShingle |
Luwen eNing Geng eLiu Guibo eLi Yong eHou Yin eTong Jiankui eHe Current Challenges in Bioinformatics of Single Cell Genomics Frontiers in Oncology SNP DNA SEQUENCING CNV single cell analysis RNA sequencing |
author_facet |
Luwen eNing Geng eLiu Guibo eLi Yong eHou Yin eTong Jiankui eHe |
author_sort |
Luwen eNing |
title |
Current Challenges in Bioinformatics of Single Cell Genomics |
title_short |
Current Challenges in Bioinformatics of Single Cell Genomics |
title_full |
Current Challenges in Bioinformatics of Single Cell Genomics |
title_fullStr |
Current Challenges in Bioinformatics of Single Cell Genomics |
title_full_unstemmed |
Current Challenges in Bioinformatics of Single Cell Genomics |
title_sort |
current challenges in bioinformatics of single cell genomics |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Oncology |
issn |
2234-943X |
publishDate |
2014-01-01 |
description |
Single cell genomics is a rapidly growing field with many new techniques emerging in the past few years. However, few bioinformatics tools specific for single cell genomics analysis are available. Single cell DNA/RNA sequencing data usually have low genome coverage and high amplification bias, which makes bioinformatics analysis challenging. Many current bioinformatics tools developed for bulk cell sequencing do not work well with single cell sequencing data. Here, we summarize current challenges in the bioinformatics analysis of single cell genomic DNA sequencing and single cell transcriptomes. These challenges include calling copy number variations, identifying mutated genes in tumor samples, reconstructing cell lineages, recovering low abundant transcripts, and improving the accuracy of quantitative analysis of transcripts. Development in single cell genomics bioinformatics analysis will promote the application of this technology to basic biology and medical research. |
topic |
SNP DNA SEQUENCING CNV single cell analysis RNA sequencing |
url |
http://journal.frontiersin.org/Journal/10.3389/fonc.2014.00007/full |
work_keys_str_mv |
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