Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Sujatha Kotte"'
Autor:
Aditya Rao, Thomas Joseph, Vangala G Saipradeep, Sujatha Kotte, Naveen Sivadasan, Rajgopal Srinivasan
Publikováno v:
PLoS ONE, Vol 15, Iss 4, p e0231728 (2020)
IntroductionPhenotype-driven rare disease gene prioritization relies on high quality curated resources containing disease, gene and phenotype annotations. However, the effectiveness of gene prioritization tools is constrained by the incomplete covera
Externí odkaz:
https://doaj.org/article/223c1bbf46bc4a2aadb4a443644a9360
Autor:
Aditya Rao, Saipradeep VG, Thomas Joseph, Sujatha Kotte, Naveen Sivadasan, Rajgopal Srinivasan
Publikováno v:
BMC Medical Genomics, Vol 11, Iss 1, Pp 1-12 (2018)
Abstract Background One of the major goals of genomic medicine is the identification of causal genomic variants in a patient and their relation to the observed clinical phenotypes. Prioritizing the genomic variants by considering only the genotype in
Externí odkaz:
https://doaj.org/article/2f226c2edccf47bc8554e5da314add54
Autor:
Vidushi Walia, Sujatha Kotte, Naveen Sivadasan, Hrishikesh Sharma, Thomas Joseph, Binuja Varma, Geetashree Mukherjee, V.G Saipradeep
Advanced image processing methods have shown promise in computational pathology, including the extraction of crucial microscopic features from histology images. Accurate detection and classification of cell nuclei from whole-slide images (WSI) play a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16a869e107c8e6dd7077e6841cf0a077
https://doi.org/10.1101/2023.05.10.540156
https://doi.org/10.1101/2023.05.10.540156
Autor:
Sujatha Kotte, VG Saipradeep, Naveen Sivadasan, Thomas Joseph, Hrishikesh Sharma, Vidushi Walia, Binuja Varma, Geetashree Mukherjee
Publikováno v:
Mitosis Domain Generalization and Diabetic Retinopathy Analysis ISBN: 9783031336577
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5b990a05477623d6b062999ff0f42c3
https://doi.org/10.1007/978-3-031-33658-4_23
https://doi.org/10.1007/978-3-031-33658-4_23
Autor:
Zhiqiang Hu, Jesse M. Hunter, Olivier Lichtarge, Sean D. Mooney, Aashish N. Adhikari, Steven E. Brenner, Rita Casadio, Yizhou Yin, Lipika R. Pal, Uma Sunderam, Panagiotis Katsonis, Predrag Radivojac, Thomas Joseph, Giulia Babbi, Naveen Sivadasan, Constantina Bakolitsa, Vangala G. Saipradeep, Laura Kasak, John Moult, Julian Gough, M. Stephen Meyn, Pier Luigi Martelli, Jennifer Poitras, Rupa A Udani, Jan Zaucha, Rafael F. Guerrero, Yuxiang Jiang, Aditya Rao, Sujatha Kotte, Kunal Kundu
Publikováno v:
Hum Mutat
Whole-genome sequencing (WGS) holds great potential as a diagnostic test. However, the majority of patients currently undergoing WGS lack a molecular diagnosis, largely due to the vast number of undiscovered disease genes and our inability to assess
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d965f4678b430bbf6815058eecb3cdf6
https://doi.org/10.1002/humu.23874
https://doi.org/10.1002/humu.23874
Autor:
Aditya Rao, VG Saipradeep, Thomas Joseph, Sujatha Kotte, Naveen Sivadasan, Rajgopal Srinivasan
Background: The COVID-19 pandemic has led to a massive and collective pursuit by the research community to find effective diagnostics, drugs and vaccines The large and growing body of literature present in MEDLINE and other online resources including
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::739a0f3d0c40ec692009070a8defd6e5
https://doi.org/10.26434/chemrxiv.12234564.v2
https://doi.org/10.26434/chemrxiv.12234564.v2
Autor:
Rajgopal Srinivasan, Vangala G. Saipradeep, Aditya Rao, Sujatha Kotte, Thomas Joseph, Naveen Sivadasan
Publikováno v:
PLoS ONE
PLoS ONE, Vol 15, Iss 4, p e0231728 (2020)
PLoS ONE, Vol 15, Iss 4, p e0231728 (2020)
IntroductionPhenotype-driven rare disease gene prioritization relies on high quality curated resources containing disease, gene and phenotype annotations. However, the effectiveness of gene prioritization tools is constrained by the incomplete covera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cb45935a56f5a9b5b9728e6ca2566c2
https://doi.org/10.1371/journal.pone.0231728
https://doi.org/10.1371/journal.pone.0231728
Autor:
Rao, Aditya, Saipradeep VG, Joseph, Thomas, Sujatha Kotte, Sivadasan, Naveen, Rajgopal Srinivasan
Rare disease clinical cases from recent publications. (PDF 139 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99888ea7f00dea8ff0348aeed0132476
Autor:
Rao, Aditya, Saipradeep VG, Joseph, Thomas, Sujatha Kotte, Sivadasan, Naveen, Rajgopal Srinivasan
Experimental Results in tabular format. (PDF 66 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ef71225ec64760beeb65fccc819dc72
Autor:
Sujatha Kotte, Naveen Sivadasan, Rajgopal Srinivasan, Aditya Rao, Thomas Joseph, Saipradeep Vg
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, Vol 11, Iss 1, Pp 1-12 (2018)
BMC Medical Genomics, Vol 11, Iss 1, Pp 1-12 (2018)
Background One of the major goals of genomic medicine is the identification of causal genomic variants in a patient and their relation to the observed clinical phenotypes. Prioritizing the genomic variants by considering only the genotype information
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab95d89e2091e887932b610e643a8f5b
https://pubmed.ncbi.nlm.nih.gov/29980210
https://pubmed.ncbi.nlm.nih.gov/29980210