Hasil Pencarian - Sayed Mohammad Ebrahim Sahraeian

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  1. 1
    SMETANA: accurate and scalable algorithm for probabilistic alignment of large-scale biological networks.

    SMETANA: accurate and scalable algorithm for probabilistic alignment of large-scale biological networks. oleh Sayed Mohammad Ebrahim Sahraeian, Byung-Jun Yoon

    Diterbitkan 2013-01-01
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  2. 2
    A network synthesis model for generating protein interaction network families.

    A network synthesis model for generating protein interaction network families. oleh Sayed Mohammad Ebrahim Sahraeian, Byung-Jun Yoon

    Diterbitkan 2012-01-01
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  3. 3
    Deep convolutional neural networks for accurate somatic mutation detection

    Deep convolutional neural networks for accurate somatic mutation detection oleh Sayed Mohammad Ebrahim Sahraeian, Ruolin Liu, Bayo Lau, Karl Podesta, Marghoob Mohiyuddin, Hugo Y. K. Lam

    Diterbitkan 2019-03-01
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  4. 4
    Achieving robust somatic mutation detection with deep learning models derived from reference data sets of a cancer sample

    Achieving robust somatic mutation detection with deep learning models derived from reference data sets of a cancer sample oleh Sayed Mohammad Ebrahim Sahraeian, Li Tai Fang, Konstantinos Karagiannis, Malcolm Moos, Sean Smith, Luis Santana-Quintero, Chunlin Xiao, Michael Colgan, Huixiao Hong, Marghoob Mohiyuddin, Wenming Xiao

    Diterbitkan 2022-01-01
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  5. 5
    Hidden biases in germline structural variant detection

    Hidden biases in germline structural variant detection oleh Michael M. Khayat, Sayed Mohammad Ebrahim Sahraeian, Samantha Zarate, Andrew Carroll, Huixiao Hong, Bohu Pan, Leming Shi, Richard A. Gibbs, Marghoob Mohiyuddin, Yuanting Zheng, Fritz J. Sedlazeck

    Diterbitkan 2021-12-01
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  6. 6
    Gaining comprehensive biological insight into the transcriptome by performing a broad-spectrum RNA-seq analysis

    Gaining comprehensive biological insight into the transcriptome by performing a broad-spectrum RNA-seq analysis oleh Sayed Mohammad Ebrahim Sahraeian, Marghoob Mohiyuddin, Robert Sebra, Hagen Tilgner, Pegah T. Afshar, Kin Fai Au, Narges Bani Asadi, Mark B. Gerstein, Wing Hung Wong, Michael P. Snyder, Eric Schadt, Hugo Y. K. Lam

    Diterbitkan 2017-07-01
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  7. 7
    Towards accurate indel calling for oncopanel sequencing through an international pipeline competition at precisionFDA

    Towards accurate indel calling for oncopanel sequencing through an international pipeline competition at precisionFDA oleh Binsheng Gong, Samir Lababidi, Rebecca Kusko, Khaled Bouri, Sarah Prezek, Vishal Thovarai, Anish Prasanna, Ezekiel J. Maier, Mahdi Golkaram, Xingqiang Sun, Konstantinos Kyriakidis, João Paulo Kitajima, Sayed Mohammad Ebrahim Sahraeian, Yunfei Guo, Elaine Johanson, Wendell Jones, Weida Tong, Joshua Xu

    Diterbitkan 2024-04-01
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  8. 8
    Assessing reproducibility of inherited variants detected with short-read whole genome sequencing

    Assessing reproducibility of inherited variants detected with short-read whole genome sequencing oleh Bohu Pan, Luyao Ren, Vitor Onuchic, Meijian Guan, Rebecca Kusko, Steve Bruinsma, Len Trigg, Andreas Scherer, Baitang Ning, Chaoyang Zhang, Christine Glidewell-Kenney, Chunlin Xiao, Eric Donaldson, Fritz J. Sedlazeck, Gary Schroth, Gokhan Yavas, Haiying Grunenwald, Haodong Chen, Heather Meinholz, Joe Meehan, Jing Wang, Jingcheng Yang, Jonathan Foox, Jun Shang, Kelci Miclaus, Lianhua Dong, Leming Shi, Marghoob Mohiyuddin, Mehdi Pirooznia, Ping Gong, Rooz Golshani, Russ Wolfinger, Samir Lababidi, Sayed Mohammad Ebrahim Sahraeian, Steve Sherry, Tao Han, Tao Chen, Tieliu Shi, Wanwan Hou, Weigong Ge, Wen Zou, Wenjing Guo, Wenjun Bao, Wenzhong Xiao, Xiaohui Fan, Yoichi Gondo, Ying Yu, Yongmei Zhao, Zhenqiang Su, Zhichao Liu, Weida Tong, Wenming Xiao, Justin M. Zook, Yuanting Zheng, Huixiao Hong

    Diterbitkan 2022-01-01
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  9. 9
    A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency

    A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency oleh Wendell Jones, Binsheng Gong, Natalia Novoradovskaya, Dan Li, Rebecca Kusko, Todd A. Richmond, Donald J. Johann, Halil Bisgin, Sayed Mohammad Ebrahim Sahraeian, Pierre R. Bushel, Mehdi Pirooznia, Katherine Wilkins, Marco Chierici, Wenjun Bao, Lee Scott Basehore, Anne Bergstrom Lucas, Daniel Burgess, Daniel J. Butler, Simon Cawley, Chia-Jung Chang, Guangchun Chen, Tao Chen, Yun-Ching Chen, Daniel J. Craig, Angela del Pozo, Jonathan Foox, Margherita Francescatto, Yutao Fu, Cesare Furlanello, Kristina Giorda, Kira P. Grist, Meijian Guan, Yingyi Hao, Scott Happe, Gunjan Hariani, Nathan Haseley, Jeff Jasper, Giuseppe Jurman, David Philip Kreil, Paweł Łabaj, Kevin Lai, Jianying Li, Quan-Zhen Li, Yulong Li, Zhiguang Li, Zhichao Liu, Mario Solís López, Kelci Miclaus, Raymond Miller, Vinay K. Mittal, Marghoob Mohiyuddin, Carlos Pabón-Peña, Barbara L. Parsons, Fujun Qiu, Andreas Scherer, Tieliu Shi, Suzy Stiegelmeyer, Chen Suo, Nikola Tom, Dong Wang, Zhining Wen, Leihong Wu, Wenzhong Xiao, Chang Xu, Ying Yu, Jiyang Zhang, Yifan Zhang, Zhihong Zhang, Yuanting Zheng, Christopher E. Mason, James C. Willey, Weida Tong, Leming Shi, Joshua Xu

    Diterbitkan 2021-04-01
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