Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Yingbo CUI"'
Autor:
Liya Zhang, Ying Hu, Min Xie, Yuxin Zhang, Kuankuan Cen, Lili Chen, Yingbo Cui, Haibo Li, Donge Wang
Publikováno v:
Journal of International Medical Research, Vol 51 (2023)
The current case report describes the clinical, biochemical and genetic characteristics of carnitine-acylcarnitine translocase deficiency (CACTD) in infant male and female twins that presented with symptoms shortly after elective caesarean delivery.
Externí odkaz:
https://doaj.org/article/7efb4027b3b44612af4e54a9f79b65b8
Autor:
Yingbo Cui, Zihang Wang, Johannes Köster, Xiangke Liao, Shaoliang Peng, Tao Tang, Chun Huang, Canqun Yang
Publikováno v:
BMC Bioinformatics, Vol 22, Iss 1, Pp 1-7 (2021)
Abstract Background VISPR is an interactive visualization and analysis framework for CRISPR screening experiments. However, it only supports the output of MAGeCK, and requires installation and manual configuration. Furthermore, VISPR is designed to r
Externí odkaz:
https://doaj.org/article/a01515760a4f42b39a97e449e9a3f3d5
Publikováno v:
BMC Genomics, Vol 21, Iss S1, Pp 1-6 (2020)
Abstract Background The Type II clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated proteins (Cas) is a powerful genome editing technology, which is more and more popular in gene function analysis. In CRISPR/Cas,
Externí odkaz:
https://doaj.org/article/72c058a938204ff895b09e8619ce4791
Autor:
Shaoliang Peng, Minxia Cheng, Kaiwen Huang, YingBo Cui, Zhiqiang Zhang, Runxin Guo, Xiaoyu Zhang, Shunyun Yang, Xiangke Liao, Yutong Lu, Quan Zou, Benyun Shi
Publikováno v:
BMC Bioinformatics, Vol 19, Iss S9, Pp 101-110 (2018)
Abstract Background Novel sequence motifs detection is becoming increasingly essential in computational biology. However, the high computational cost greatly constrains the efficiency of most motif discovery algorithms. Results In this paper, we acce
Externí odkaz:
https://doaj.org/article/608ffd9dab7a4d5bac7bd3d42e7a7973
Publikováno v:
大数据, Vol 6, Pp 2020041-1 (2020)
Sequence alignment and mutation detection are the basic steps of genomic data analysis.They are the premise of subsequent functional analysis,and the most time-consuming steps.In order to effectively deal with the massive genomic big data brought by
Externí odkaz:
https://doaj.org/article/3edb2067b564450fb2715c0091d6e8f4
Autor:
Shaoliang PENG, Shunyun YANG, Zhe SUN, Minxia CHENG, Yingbo CUI, Xiaowei WANG, Fei LI, Xiaochen BO, Xiangke LIAO
Publikováno v:
大数据, Vol 4, p 2018027 (2018)
The biological assessment,including matching algorithm,is realized by measuring and analyzing the human cells’ transcription reaction after stimulated by biological agents,to quickly determine the relevant detection markers and treatment targets.Si
Externí odkaz:
https://doaj.org/article/d80bedb0c5624069884465b872488a9f
Publikováno v:
2022 IEEE International Conference on Bioinformatics and Biomedicine (BIBM).
Publikováno v:
Interdisciplinary Sciences, Computational Life Sciences
The rapid advances in sequencing technology have led to an explosion of sequence data. Sequence alignment is the central and fundamental problem in many sequence analysis procedure, while local alignment is often the kernel of these algorithms. Usual
MinimapR: A parallel alignment tool for the analysis of large-scale third-generation sequencing data
Publikováno v:
Computational biology and chemistry. 99
The development of third-generation sequencing technology has brought significant changes and influences on genomics. Compared to the second-generation sequencing methods, the third-generation technologies produce around 100 times longer reads to rev
Autor:
Jijun Yu, Wubing Zhang, Zexiang Zeng, Yuan Gao, Xiaolong Cheng, Yingbo Cui, Tyson Dawson, Shaoliang Peng, Wei Li, Bicna Song, Lumen Chao, Teng Fei, Dian Li, Qing Chen, Anthony Chiu, Zexu Li
Publikováno v:
Nucleic Acids Research
High-throughput genetic screening based on CRISPR/Cas9 or RNA-interference (RNAi) enables the exploration of genes associated with the phenotype of interest on a large scale. The rapid accumulation of public available genetic screening data provides