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dc.contributor.authorFraenkel, Ernest
dc.date.accessioned2023-01-31T18:23:17Z
dc.date.available2023-01-31T18:23:17Z
dc.date.issued2022
dc.identifier.urihttps://hdl.handle.net/1721.1/147814
dc.description.abstract<jats:title>Abstract</jats:title><jats:p>Answer ALS is a biological and clinical resource of patient-derived, induced pluripotent stem (iPS) cell lines, multi-omic data derived from iPS neurons and longitudinal clinical and smartphone data from over 1,000 patients with ALS. This resource provides population-level biological and clinical data that may be employed to identify clinical–molecular–biochemical subtypes of amyotrophic lateral sclerosis (ALS). A unique smartphone-based system was employed to collect deep clinical data, including fine motor activity, speech, breathing and linguistics/cognition. The iPS spinal neurons were blood derived from each patient and these cells underwent multi-omic analytics including whole-genome sequencing, RNA transcriptomics, ATAC-sequencing and proteomics. The intent of these data is for the generation of integrated clinical and biological signatures using bioinformatics, statistics and computational biology to establish patterns that may lead to a better understanding of the underlying mechanisms of disease, including subgroup identification. A web portal for open-source sharing of all data was developed for widespread community-based data analytics.</jats:p>en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionof10.1038/S41593-021-01006-0en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNatureen_US
dc.titleAnswer ALS, a large-scale resource for sporadic and familial ALS combining clinical and multi-omics data from induced pluripotent cell linesen_US
dc.typeArticleen_US
dc.identifier.citationFraenkel, Ernest. 2022. "Answer ALS, a large-scale resource for sporadic and familial ALS combining clinical and multi-omics data from induced pluripotent cell lines." Nature Neuroscience, 25 (2).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.relation.journalNature Neuroscienceen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2023-01-31T18:19:14Z
dspace.orderedauthorsBaxi, EG; Thompson, T; Li, J; Kaye, JA; Lim, RG; Wu, J; Ramamoorthy, D; Lima, L; Vaibhav, V; Matlock, A; Frank, A; Coyne, AN; Landin, B; Ornelas, L; Mosmiller, E; Thrower, S; Farr, SM; Panther, L; Gomez, E; Galvez, E; Perez, D; Meepe, I; Lei, S; Mandefro, B; Trost, H; Pinedo, L; Banuelos, MG; Liu, C; Moran, R; Garcia, V; Workman, M; Ho, R; Wyman, S; Roggenbuck, J; Harms, MB; Stocksdale, J; Miramontes, R; Wang, K; Venkatraman, V; Holewenski, R; Sundararaman, N; Pandey, R; Manalo, D-M; Donde, A; Huynh, N; Adam, M; Wassie, BT; Vertudes, E; Amirani, N; Raja, K; Thomas, R; Hayes, L; Lenail, A; Cerezo, A; Luppino, S; Farrar, A; Pothier, L; Prina, C; Morgan, T; Jamil, A; Heintzman, S; Jockel-Balsarotti, J; Karanja, E; Markway, J; McCallum, M; Joslin, B; Alibazoglu, D; Kolb, S; Ajroud-Driss, S; Baloh, R; Heitzman, D; Miller, T; Glass, JD; Patel-Murray, NL; Yu, H; Sinani, E; Vigneswaran, P; Sherman, AV; Ahmad, O; Roy, P; Beavers, JC; Zeiler, S; Krakauer, JW; Agurto, C; Cecchi, G; Bellard, M; Raghav, Y; Sachs, K; Ehrenberger, T; Bruce, E; Cudkowicz, ME; Maragakis, N; Norel, R; Van Eyk, JE; Finkbeiner, S; Berry, J; Sareen, D; Thompson, LM; Fraenkel, E; Svendsen, CN; Rothstein, JDen_US
dspace.date.submission2023-01-31T18:19:21Z
mit.journal.volume25en_US
mit.journal.issue2en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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