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

Comparative analysis of RNA expression in a single institution cohort of pediatric cancer patients

对单中心儿科癌症患者队列的RNA表达进行比较分析

Vasquez, Yvonne A; Beale, Holly C; Sanders, Lauren; Lyle, A Geoffrey; Kephart, Ellen T; Learned, Katrina; Thompson, Drew; Peralez, Jennifer; Li, Amy; Huang, Min; Pyke-Grimm, Kimberly A; Salama, Sofie R; Haussler, David; Bjork, Isabel; Sheri, L Spunt; Vaske, Olena M

Comparative analysis of RNA expression identifies effective targeted drug in myoepithelial carcinoma

RNA表达的比较分析可识别肌上皮癌中的有效靶向药物

Vasquez, Yvonne A; Sanders, Lauren; Beale, Holly C; Lyle, A Geoffrey; Kephart, Ellen T; Learned, Katrina; Peralez, Jennifer; Li, Amy; Huang, Min; Pyke-Grimm, Kimberly A; Tan, Serena Y; Salama, Sofie R; Haussler, David; Bjork, Isabel; Vaske, Olena M; Spunt, Sheri L

Consistently processed RNA sequencing data from 50 sources enriched for pediatric data

一致处理的来自 50 个来源的 RNA 测序数据,其中儿科数据尤为丰富。

Beale, Holly C; Learned, Katrina; Kephart, Ellen T; Lyle, A Geoffrey; van den Bout, Anouk; McCabe, Molly; Echandia-Monroe, Kathryn; Khare, Mansi J; Huang, Elise Y; Jariwala, Sneha; Antilla, Reyna; Cheney, Allison; Lee, Alex G; Sayles, Leanne C; Leung, Stanley G; Vasquez, Yvonne A; Sanders, Lauren; Haussler, David; Salama, Sofie R; Sweet-Cordero, E Alejandro; Vaske, Olena M

A novel splice site variant in DEGS1 leads to aberrant splicing and loss of DEGS1 enzyme activity, a VUS resolved.

DEGS1 中的一种新型剪接位点变异导致异常剪接和 DEGS1 酶活性丧失,这是一个已解决的 VUS

Beale Holly C, Tse Victor, Lee Joanna Y, Akutagawa Jon, Mavura Yusuph, Saint-John Brandon, Cheney Allison, Mulligan Dennis R, Chacaltana Guillermo, Gutierrez Martin, Tenney Jessica, Shieh Joseph T, Martin Pierre-Marie, Yip Tiffany, Hodoglugil Ugur, Fay Alex J, Brooks Angela N, Van Ziffle Jessica, Stone Michael D, Risch Neil, Sanford Jeremy R, Devine Patrick, Saba Julie D, Vaske Olena M, Slavotinek Anne

TPP1 promoter mutations cooperate with TERT promoter mutations to lengthen telomeres in melanoma

TPP1启动子突变与TERT启动子突变协同作用,延长黑色素瘤中的端粒。

Chun-On, Pattra; Hinchie, Angela M; Beale, Holly C; Gil Silva, Agustin A; Rush, Elizabeth; Sander, Cindy; Connelly, Carla J; Seynnaeve, Brittani K N; Kirkwood, John M; Vaske, Olena M; Greider, Carol W; Alder, Jonathan K

Machine learning multi-omics analysis reveals cancer driver dysregulation in pan-cancer cell lines compared to primary tumors

机器学习多组学分析揭示泛癌细胞系与原发肿瘤相比存在癌症驱动基因失调

Sanders, Lauren M; Chandra, Rahul; Zebarjadi, Navid; Beale, Holly C; Lyle, A Geoffrey; Rodriguez, Analiz; Kephart, Ellen Towle; Pfeil, Jacob; Cheney, Allison; Learned, Katrina; Currie, Rob; Gitlin, Leonid; Vengerov, David; Haussler, David; Salama, Sofie R; Vaske, Olena M

Hydra: A mixture modeling framework for subtyping pediatric cancer cohorts using multimodal gene expression signatures

Hydra:一种利用多模态基因表达特征对儿童癌症队列进行亚型分类的混合模型框架

Pfeil, Jacob; Sanders, Lauren M; Anastopoulos, Ioannis; Lyle, A Geoffrey; Weinstein, Alana S; Xue, Yuanqing; Blair, Andrew; Beale, Holly C; Lee, Alex; Leung, Stanley G; Dinh, Phuong T; Shah, Avanthi Tayi; Breese, Marcus R; Devine, W Patrick; Bjork, Isabel; Salama, Sofie R; Sweet-Cordero, E Alejandro; Haussler, David; Vaske, Olena Morozova

Bayesian Framework for Detecting Gene Expression Outliers in Individual Samples

基于贝叶斯框架的个体样本基因表达异常值检测

Vivian, John; Eizenga, Jordan M; Beale, Holly C; Vaske, Olena M; Paten, Benedict

Whole genome sequencing in cats, identifies new models for blindness in AIPL1 and somite segmentation in HES7

对猫进行全基因组测序,发现了AIPL1基因中导致失明和HES7基因中导致体节分割的新模型。

Lyons, Leslie A; Creighton, Erica K; Alhaddad, Hasan; Beale, Holly C; Grahn, Robert A; Rah, HyungChul; Maggs, David J; Helps, Christopher R; Gandolfi, Barbara

Leading the way: finding genes for neurologic disease in dogs using genome-wide mRNA sequencing

引领潮流:利用全基因组mRNA测序寻找犬类神经系统疾病基因

Ostrander, Elaine A; Beale, Holly C