A Bioinformatics Approach for Determining Sample Identity from Different Lanes of High-Throughput Sequencing Data

por Goldfeder, Rachel L., Parker, Stephen C. J., Ajay, Subramanian S., Ozel Abaan, Hatice, Margulies, Elliott H.
Publicado 2011

Mining Twitter Data to Improve Detection of Schizophrenia

por McManus, Kimberly, Mallory, Emily K., Goldfeder, Rachel L., Haynes, Winston A., Tatum, Jonathan D.
Publicado en AMIA Jt Summits Transl Sci Proc (2015)

Human Genome Sequencing at the Population Scale: A Primer on High-Throughput DNA Sequencing and Analysis

por Goldfeder, Rachel L, Wall, Dennis P, Khoury, Muin J, Ioannidis, John P A, Ashley, Euan A
Publicado en Am J Epidemiol (2017)

An Evaluation Framework for Lossy Compression of Genome Sequencing Quality Values

por Alberti, Claudio, Daniels, Noah, Hernaez, Mikel, Voges, Jan, Goldfeder, Rachel L., Hernandez-Lopez, Ana A., Mattavelli, Marco, Berger, Bonnie
Publicado en Proc Data Compress Conf (2016)

Modeling Drosophila Positional Preferences in Open Field Arenas with Directional Persistence and Wall Attraction

por Soibam, Benjamin, Goldfeder, Rachel L., Manson-Bishop, Claire, Gamblin, Rachel, Pletcher, Scott D., Shah, Shishir, Gunaratne, Gemunu H., Roman, Gregg W.
Publicado 2012

Correction: Modeling Drosophila Positional Preferences in Open Field Arenas with Directional Persistence and Wall Attraction

por Soibam, Benjamin, Goldfeder, Rachel L., Manson-Bishop, Claire, Gamblin, Rachel, Pletcher, Scott D., Shah, Shishir, Gunaratne, Gemunu H., Roman, Gregg W.
Publicado 2012

Medical implications of technical accuracy in genome sequencing

por Goldfeder, Rachel L., Priest, James R., Zook, Justin M., Grove, Megan E., Waggott, Daryl, Wheeler, Matthew T., Salit, Marc, Ashley, Euan A.
Publicado en Genome Med (2016)

Differential immune profiles distinguish the mutational subtypes of gastrointestinal stromal tumor

por Vitiello, Gerardo A., Bowler, Timothy G., Liu, Mengyuan, Medina, Benjamin D., Zhang, Jennifer Q., Param, Nesteene J., Loo, Jennifer K., Goldfeder, Rachel L., Chibon, Frederic, Rossi, Ferdinand, Zeng, Shan, DeMatteo, Ronald P.
Publicado en J Clin Invest (2019)

Chromatin Interaction Analyses Elucidate PRC2-bound Silencers’ Roles in Mouse Development

por Ngan, Chew Yee, Wong, Chee Hong, Tjong, Harianto, Wang, Wenbo, Goldfeder, Rachel L., Choi, Cindy, He, Hao, Gong, Liang, Lin, Junyan, Urban, Barbara, Chow, Julianna, Li, Meihong, Lim, Joanne, Philip, Vivek, Murray, Stephen A., Wang, Haoyi, Wei, Chia-Lin
Publicado en Nat Genet (2020)

Autosomal Dominant Diabetes Arising From a Wolfram Syndrome 1 Mutation

por Bonnycastle, Lori L., Chines, Peter S., Hara, Takashi, Huyghe, Jeroen R., Swift, Amy J., Heikinheimo, Pirkko, Mahadevan, Jana, Peltonen, Sirkku, Huopio, Hanna, Nuutila, Pirjo, Narisu, Narisu, Goldfeder, Rachel L., Stitzel, Michael L., Lu, Simin, Boehnke, Michael, Urano, Fumihiko, Collins, Francis S., Laakso, Markku
Publicado 2013

Clinical Interpretation and Implications of Whole-Genome Sequencing

por Dewey, Frederick E., Grove, Megan E., Pan, Cuiping, Goldstein, Benjamin A., Bernstein, Jonathan A., Chaib, Hassan, Merker, Jason D., Goldfeder, Rachel L., Enns, Gregory M., David, Sean P., Pakdaman, Neda, Ormond, Kelly E., Caleshu, Colleen, Kingham, Kerry, Klein, Teri E., Whirl-Carrillo, Michelle, Sakamoto, Kenneth, Wheeler, Matthew T., Butte, Atul J., Ford, James M., Boxer, Linda, Ioannidis, John P. A., Yeung, Alan C., Altman, Russ B., Assimes, Themistocles L., Snyder, Michael, Ashley, Euan A., Quertermous, Thomas
Publicado 2014