日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

nf-core/airrflow: An adaptive immune receptor repertoire analysis workflow employing the Immcantation framework

nf-core/airrflow:一种采用 Immcantation 框架的适应性免疫受体库分析工作流程

Gabernet, Gisela; Marquez, Susanna; Bjornson, Robert; Peltzer, Alexander; Meng, Hailong; Aron, Edel; Lee, Noah Y; Jensen, Cole G; Ladd, David; Polster, Mark; Hanssen, Friederike; Heumos, Simon; Yaari, Gur; Kowarik, Markus C; Nahnsen, Sven; Kleinstein, Steven H

Using blockchain to log genome dataset access: efficient storage and query

利用区块链记录基因组数据集访问:高效的存储和查询

Gürsoy, Gamze; Bjornson, Robert; Green, Molly E; Gerstein, Mark

De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus

人类先天性脑积水中调控神经干细胞命运的基因发生新生突变

Furey, Charuta Gavankar; Choi, Jungmin; Jin, Sheng Chih; Zeng, Xue; Timberlake, Andrew T; Nelson-Williams, Carol; Mansuri, M Shahid; Lu, Qiongshi; Duran, Daniel; Panchagnula, Shreyas; Allocco, August; Karimy, Jason K; Khanna, Arjun; Gaillard, Jonathan R; DeSpenza, Tyrone; Antwi, Prince; Loring, Erin; Butler, William E; Smith, Edward R; Warf, Benjamin C; Strahle, Jennifer M; Limbrick, David D; Storm, Phillip B; Heuer, Gregory; Jackson, Eric M; Iskandar, Bermans J; Johnston, James M; Tikhonova, Irina; Castaldi, Christopher; López-Giráldez, Francesc; Bjornson, Robert D; Knight, James R; Bilguvar, Kaya; Mane, Shrikant; Alper, Seth L; Haider, Shozeb; Guclu, Bulent; Bayri, Yasar; Sahin, Yener; Apuzzo, Michael L J; Duncan, Charles C; DiLuna, Michael L; Günel, Murat; Lifton, Richard P; Kahle, Kristopher T

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

2871例先天性心脏病先证者中罕见遗传变异和新发变异的贡献

Jin, Sheng Chih; Homsy, Jason; Zaidi, Samir; Lu, Qiongshi; Morton, Sarah; DePalma, Steven R; Zeng, Xue; Qi, Hongjian; Chang, Weni; Sierant, Michael C; Hung, Wei-Chien; Haider, Shozeb; Zhang, Junhui; Knight, James; Bjornson, Robert D; Castaldi, Christopher; Tikhonoa, Irina R; Bilguvar, Kaya; Mane, Shrikant M; Sanders, Stephan J; Mital, Seema; Russell, Mark W; Gaynor, J William; Deanfield, John; Giardini, Alessandro; Porter, George A Jr; Srivastava, Deepak; Lo, Cecelia W; Shen, Yufeng; Watkins, W Scott; Yandell, Mark; Yost, H Joseph; Tristani-Firouzi, Martin; Newburger, Jane W; Roberts, Amy E; Kim, Richard; Zhao, Hongyu; Kaltman, Jonathan R; Goldmuntz, Elizabeth; Chung, Wendy K; Seidman, Jonathan G; Gelb, Bruce D; Seidman, Christine E; Lifton, Richard P; Brueckner, Martina

Large-Scale trans-eQTLs Affect Hundreds of Transcripts and Mediate Patterns of Transcriptional Co-regulation

大规模反式eQTL影响数百个转录本并介导转录共调控模式

Brynedal, Boel; Choi, JinMyung; Raj, Towfique; Bjornson, Robert; Stranger, Barbara E; Neale, Benjamin M; Voight, Benjamin F; Cotsapas, Chris

Korean Variant Archive (KOVA): a reference database of genetic variations in the Korean population

韩国变异档案库(KOVA):韩国人群遗传变异的参考数据库

Lee, Sangmoon; Seo, Jihae; Park, Jinman; Nam, Jae-Yong; Choi, Ahyoung; Ignatius, Jason S; Bjornson, Robert D; Chae, Jong-Hee; Jang, In-Jin; Lee, Sanghyuk; Park, Woong-Yang; Baek, Daehyun; Choi, Murim

YPED: an integrated bioinformatics suite and database for mass spectrometry-based proteomics research

YPED:用于基于质谱的蛋白质组学研究的集成生物信息学套件和数据库

Colangelo, Christopher M; Shifman, Mark; Cheung, Kei-Hoi; Stone, Kathryn L; Carriero, Nicholas J; Gulcicek, Erol E; Lam, TuKiet T; Wu, Terence; Bjornson, Robert D; Bruce, Can; Nairn, Angus C; Rinehart, Jesse; Miller, Perry L; Williams, Kenneth R

A spatial simulation approach to account for protein structure when identifying non-random somatic mutations.

在识别非随机体细胞突变时,采用空间模拟方法来考虑蛋白质结构

Ryslik Gregory A, Cheng Yuwei, Cheung Kei-Hoi, Bjornson Robert D, Zelterman Daniel, Modis Yorgo, Zhao Hongyu

Comparative genomics reveals multiple genetic backgrounds of human pathogenicity in the Trypanosoma brucei complex

比较基因组学揭示了布氏锥虫复合体人类致病性的多种遗传背景

Sistrom, Mark; Evans, Benjamin; Bjornson, Robert; Gibson, Wendy; Balmer, Oliver; Mäser, Pascal; Aksoy, Serap; Caccone, Adalgisa

De novo mutations in histone-modifying genes in congenital heart disease

先天性心脏病中组蛋白修饰基因的新生突变

Zaidi, Samir; Choi, Murim; Wakimoto, Hiroko; Ma, Lijiang; Jiang, Jianming; Overton, John D; Romano-Adesman, Angela; Bjornson, Robert D; Breitbart, Roger E; Brown, Kerry K; Carriero, Nicholas J; Cheung, Yee Him; Deanfield, John; DePalma, Steve; Fakhro, Khalid A; Glessner, Joseph; Hakonarson, Hakon; Italia, Michael J; Kaltman, Jonathan R; Kaski, Juan; Kim, Richard; Kline, Jennie K; Lee, Teresa; Leipzig, Jeremy; Lopez, Alexander; Mane, Shrikant M; Mitchell, Laura E; Newburger, Jane W; Parfenov, Michael; Pe'er, Itsik; Porter, George; Roberts, Amy E; Sachidanandam, Ravi; Sanders, Stephan J; Seiden, Howard S; State, Mathew W; Subramanian, Sailakshmi; Tikhonova, Irina R; Wang, Wei; Warburton, Dorothy; White, Peter S; Williams, Ismee A; Zhao, Hongyu; Seidman, Jonathan G; Brueckner, Martina; Chung, Wendy K; Gelb, Bruce D; Goldmuntz, Elizabeth; Seidman, Christine E; Lifton, Richard P