The research of ARIMA, GM(1,1), and LSTM models for prediction of TB cases in China
Zhao, Daren, Zhang, Huiwu, Cao, Qing, Wang, Zhiyi, He, Sizhang, Zhou, Minghua, Zhang, Ruihua
Published in PloS one (23.02.2022)
Published in PloS one (23.02.2022)
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Journal Article
Spatial and temporal analysis and forecasting of TB reported incidence in western China
Zhao, Daren, Zhang, Huiwu, Wu, Xuelian, Zhang, Lan, Li, Shiyuan, He, Sizhang
Published in BMC public health (13.09.2024)
Published in BMC public health (13.09.2024)
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Journal Article
The research of SARIMA model for prediction of hepatitis B in mainland China
Zhao, Daren, Zhang, Huiwu, Cao, Qing, Wang, Zhiyi, Zhang, Ruihua
Published in Medicine (Baltimore) (10.06.2022)
Published in Medicine (Baltimore) (10.06.2022)
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Journal Article
FertilityOnline: A Straightforward Pipeline for Functional Gene Annotation and Disease Mutation Discovery
Gao, Jianing, Zhang, Huan, Jiang, Xiaohua, Ali, Asim, Zhao, Daren, Bao, Jianqiang, Jiang, Long, Iqbal, Furhan, Shi, Qinghua, Zhang, Yuanwei
Published in Genomics, proteomics & bioinformatics (01.06.2022)
Published in Genomics, proteomics & bioinformatics (01.06.2022)
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Journal Article
Novel Loss-of-Function Mutations in DNAH1 Displayed Different Phenotypic Spectrum in Humans and Mice
Khan, Ranjha, Zaman, Qumar, Chen, Jing, Khan, Manan, Ma, Ao, Zhou, Jianteng, Zhang, Beibei, Ali, Asim, Naeem, Muhammad, Zubair, Muhammad, Zhao, Daren, Shah, Wasim, Khan, Mazhar, Zhang, Yuanwei, Xu, Bo, Zhang, Huan, Shi, Qinghua
Published in Frontiers in endocrinology (Lausanne) (17.11.2021)
Published in Frontiers in endocrinology (Lausanne) (17.11.2021)
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Journal Article
Biallelic Variants in CFAP61 Cause Multiple Morphological Abnormalities of the Flagella and Male Infertility
Ma, Ao, Zeb, Aurang, Ali, Imtiaz, Zhao, Daren, Khan, Asad, Zhang, Beibei, Zhou, Jianteng, Khan, Ranjha, Zhang, Huan, Zhang, Yuanwei, Khan, Ihsan, Shah, Wasim, Ali, Haider, Javed, Abdul Rafay, Ma, Hui, Shi, Qinghua
Published in Frontiers in cell and developmental biology (31.01.2022)
Published in Frontiers in cell and developmental biology (31.01.2022)
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Journal Article
MeiosisOnline: A Manually Curated Database for Tracking and Predicting Genes Associated With Meiosis
Jiang, Xiaohua, Zhao, Daren, Ali, Asim, Xu, Bo, Liu, Wei, Wen, Jie, Zhang, Huan, Shi, Qinghua, Zhang, Yuanwei
Published in Frontiers in cell and developmental biology (13.08.2021)
Published in Frontiers in cell and developmental biology (13.08.2021)
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Journal Article
Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and mice
Ma, Ao, Zhou, Jianteng, Ali, Haider, Abbas, Tanveer, Ali, Imtiaz, Muhammad, Zubair, Dil, Sobia, Chen, Jing, Huang, Xiongheng, Ma, Hui, Zhao, Daren, Zhang, Beibei, Zhang, Yuanwei, Shah, Wasim, Shah, Basit, Murtaza, Ghulam, Iqbal, Furhan, Khan, Muzammil Ahmad, Khan, Asad, Li, Qing, Xu, Bo, Wu, Limin, Zhang, Huan, Shi, Qinghua
Published in JCI insight (08.02.2023)
Published in JCI insight (08.02.2023)
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Journal Article
Loss-of-function variants in KCTD19 cause non-obstructive azoospermia in humans
Liu, Junyan, Rahim, Fazal, Zhou, Jianteng, Fan, Suixing, Jiang, Hanwei, Yu, Changping, Chen, Jing, Xu, Jianze, Yang, Gang, Shah, Wasim, Zubair, Muhammad, Khan, Asad, Li, Yang, Shah, Basit, Zhao, Daren, Iqbal, Furhan, Jiang, Xiaohua, Guo, Tonghang, Xu, Peng, Xu, Bo, Wu, Limin, Ma, Hui, Zhang, Yuanwei, Zhang, Huan, Shi, Qinghua
Published in iScience (21.07.2023)
Published in iScience (21.07.2023)
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Journal Article
The research of ARIMA, GM
Zhao, Daren, Zhang, Huiwu, Cao, Qing, Wang, Zhiyi, He, Sizhang, Zhou, Minghua, Zhang, Ruihua
Published in PloS one (23.02.2022)
Published in PloS one (23.02.2022)
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Journal Article
PedMiner: a tool for linkage analysis-based identification of disease-associated variants using family based whole-exome sequencing data
Zhou, Jianteng, Gao, Jianing, Zhang, Huan, Zhao, Daren, Li, Ao, Iqbal, Furhan, Shi, Qinghua, Zhang, Yuanwei
Published in Briefings in bioinformatics (20.05.2021)
Published in Briefings in bioinformatics (20.05.2021)
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Journal Article
Novel frameshift mutation in STK33 is associated with asthenozoospermia and multiple morphological abnormalities of the flagella
Ma, Hui, Zhang, Beibei, Khan, Asad, Zhao, Daren, Ma, Ao, Zhou, Jianteng, Khan, Ihsan, Khan, Khalid, Zhang, Huan, Zhang, Yuanwei, Jiang, Xiaohua, Dil, Sobia, Zeb, Aurang, Rahim, Fazal, Shi, Qinghua
Published in Human molecular genetics (13.10.2021)
Published in Human molecular genetics (13.10.2021)
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Journal Article
A recessive ACTL7A founder variant leads to male infertility due to acrosome detachment in Pakistani Pashtuns
Zhou, Jianteng, Zhang, Beibei, Zeb, Aurang, Ma, Ao, Chen, Jing, Zhao, Daren, Rahim, Fazal, Khan, Ranjha, Zhang, Huan, Zhang, Yuanwei, Khan, Ihsan, Kakakhel, Mian Basit Shah, Khan, Asad, Shah, Wasim, Jiang, Xiaohua, Zhang, Feng, Yang, Xiaoyu, Xiao, Jun, Xu, Bo, Ma, Hui, Shi, Qinghua
Published in Clinical genetics (01.11.2023)
Published in Clinical genetics (01.11.2023)
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Journal Article
Fertility Online:A Straightforward Pipeline for Functional Gene Annotation and Disease Mutation Discovery
Jianing Gao, Huan Zhang, Xiaohua Jiang, Asim Ali, Daren Zhao, Jianqiang Bao, Long Jiang, Furhan Iqbal, Qinghua Shi, Yuanwei Zhang
Published in 基因组蛋白质组与生物信息学报(英文版) (2022)
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Published in 基因组蛋白质组与生物信息学报(英文版) (2022)
Journal Article
The research of ARIMA, GM(1,1), and LSTM models for prediction of TB cases in China
Daren Zhao, Huiwu Zhang, Qing Cao, Zhiyi Wang, Sizhang He, Minghua Zhou, Ruihua Zhang
Published in PloS one (01.01.2022)
Published in PloS one (01.01.2022)
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Journal Article