Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Minothi Parulekar"'
Autor:
Maria Ximena Sosa, I K Ashok Sivakumar, Samantha Maragh, Vamsi Veeramachaneni, Ramesh Hariharan, Minothi Parulekar, Karin M Fredrikson, Timothy T Harkins, Jeffrey Lin, Andrew B Feldman, Pramila Tata, Georg B Ehret, Aravinda Chakravarti
Publikováno v:
PLoS Computational Biology, Vol 8, Iss 10, p e1002737 (2012)
We describe methods for rapid sequencing of the entire human mitochondrial genome (mtgenome), which involve long-range PCR for specific amplification of the mtgenome, pyrosequencing, quantitative mapping of sequence reads to identify sequence variant
Externí odkaz:
https://doaj.org/article/1bf1abfb3b8d4eb796a4ed4b445b9237
Autor:
Avshesh Mishra, Minothi Parulekar, Anaita Udwadia Hegde, Ratna Dua Puri, Vamsi Veeramachaneni, T C Thyagarajan, M. Pradeep Kumar, Sheela Nampoothiri, Swetha Nayanala, Ramshekhar N. Menon, Soumya Sundaram, Vijayashree Gauribidanur Raghavendrachar, Mukunth Sadagopan, Frenny Sheth, Swathi M Chinnappa, Sobha George, Priyanka Kumar, Vykuntaraju K Gowda, Megha Rani Soni, Qurratulain Hasan, A. Radha Rama Devi, Neeta A. Naik, Preetha Tilak, Aparajit Sridharan, Vrajesh Udani, Ramesh Hariharan, Shanmukh Katragadda, Mahesh Kamate, S L Aswathy, Irene Rosita Pia Patric, Divya Pachat, Ashraf U Mannan, Vijay Chandru, Krati Shah, Aparna Ganapathy, H K Vidya, Mohandas Nair, Jayesh Sheth, Manasa B Prakash, Pooja Agrawal, Anil Vittal Kanthi, P A Mohammed Kunju
Publikováno v:
Journal of Neurology. 266:1919-1926
Neurological disorders are clinically heterogeneous group of disorders and are major causes of disability and death. Several of these disorders are caused due to genetic aberration. A precise and confirmatory diagnosis in the patients in a timely man
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::319986a66cf1183595f993aa250f6413
https://doi.org/10.1007/s00415-019-09358-1
https://doi.org/10.1007/s00415-019-09358-1
Autor:
Ramesh Hariharan, Vikram Vittal, Cary J. Buresh, Weiming Shen, Belen Robolledo, Pooja Agrawal, Kenneth R. Eyring, Jemima Jacob, Arun K Hariharan, Sai A. Balaji, Preveen Ramamoorthy, Minothi Parulekar, Gouri Deshpande, Shanmukh Katragadda, Aarthi Ravichandran, Ashwini Shanmugam, Urvashi Bahadur, Kalyanasundaram Subramanian, Kiran Kumari, Sravanthi Parchuru, Vijayashree Gauribidanur Raghavendrachar, Vaijayanti Gupta, Mohammed Oomer Farooque, Smita Agarwal, Divya Vishwanath, Kalpana Dhanuskodi, Vamsi Veeramachaneni, Satish Gupta, Swetha Nayanala, Qiaoling Liang, Satish Sankaran, Melanie Phooi Nee Yong, Manimala Sen
Publikováno v:
Cancer Medicine
Comprehensive genetic profiling of tumors using next‐generation sequencing (NGS) is gaining acceptance for guiding treatment decisions in cancer care. We designed a cancer profiling test combining both deep sequencing and immunohistochemistry (IHC)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::355a3e37da4838a5973554a85d38d395
https://pubmed.ncbi.nlm.nih.gov/28371134
https://pubmed.ncbi.nlm.nih.gov/28371134
Autor:
Armand M. Makowski, Minothi Parulekar
Publikováno v:
Queueing Systems. 27:271-296
The infinite server model of Cox with arbitrary service time distribution appears to provide a large class of traffic models – Pareto and log-normal distributions have already been reported in the literature for several applications. Here we begin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76dffa412748d6f25ea985c9679d095d
https://doi.org/10.1023/a:1019122400632
https://doi.org/10.1023/a:1019122400632
Autor:
Samantha Maragh, Minothi Parulekar, Aravinda Chakravarti, Karin M. Fredrikson, Maria X. Sosa, Pramila Tata, Vamsi Veeramachaneni, Georg Ehret, I K Ashok Sivakumar, Andrew B. Feldman, Ramesh Hariharan, Jeffrey S. Lin, Timothy T. Harkins
Publikováno v:
PLOS Computational Biology, Vol. 8, No 10 (2012) P. e1002737
PLoS Computational Biology
PLoS Computational Biology, Vol 8, Iss 10, p e1002737 (2012)
PLoS Computational Biology
PLoS Computational Biology, Vol 8, Iss 10, p e1002737 (2012)
We describe methods for rapid sequencing of the entire human mitochondrial genome (mtgenome), which involve long-range PCR for specific amplification of the mtgenome, pyrosequencing, quantitative mapping of sequence reads to identify sequence variant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dd5ce02d5dcf7b62df4cb2883daa2bd
https://archive-ouverte.unige.ch/unige:32235
https://archive-ouverte.unige.ch/unige:32235
Autor:
Ramesh Hariharan, Goutham Hv, Kalyanasundaram Subramanian, Minothi Parulekar, Preveen Ramamoorthy, Suman Kapoor, Manimala Sen, Vamsi Veeramachaneni, Vikram Vitthal, Urvashi Bahadur, Manasa B.P., N.S.N Swetha, Melanie Phooi Nee Yong, Satish Sankaran, Smita Agarwal, Vaijayanti Gupta, Jamuna Yadhav, Shanmukh Katragadda, Gouri Deshpande, Weiming Shen
Publikováno v:
Journal of Clinical Oncology. 33:e12539-e12539
e12539 Background: Personalized cancer treatment can benefit from targeted deep-sequencing of multiple genes using NGS. The StrandAdvantage test panel assays 212 amplicons (48 genes) spanning hotsp...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ecac4519dc62f8c4b4c1ca22af66973
https://doi.org/10.1200/jco.2015.33.15_suppl.e12539
https://doi.org/10.1200/jco.2015.33.15_suppl.e12539
Autor:
Armand M. Makowski, Minothi Parulekar
Publikováno v:
Self-Similar Network Traffic and Performance Evaluation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f21781df857741c86d26d1f38d30c28
https://doi.org/10.1002/047120644x.ch9
https://doi.org/10.1002/047120644x.ch9
Conference
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Conference
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