Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Raman Sethi"'
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-16 (2024)
Abstract ezSingleCell is an interactive and easy-to-use application for analysing various single-cell and spatial omics data types without requiring prior programing knowledge. It combines the best-performing publicly available methods for in-depth d
Externí odkaz:
https://doaj.org/article/5826d8a4b10044c896564e8e921580ca
Autor:
Hang Xu, Huazhu Fu, Yahui Long, Kok Siong Ang, Raman Sethi, Kelvin Chong, Mengwei Li, Rom Uddamvathanak, Hong Kai Lee, Jingjing Ling, Ao Chen, Ling Shao, Longqi Liu, Jinmiao Chen
Publikováno v:
Genome Medicine, Vol 16, Iss 1, Pp 1-15 (2024)
Abstract Optimal integration of transcriptomics data and associated spatial information is essential towards fully exploiting spatial transcriptomics to dissect tissue heterogeneity and map out inter-cellular communications. We present SEDR, which us
Externí odkaz:
https://doaj.org/article/a8125adae2f14b7d8fa5d78ddce5cfbd
Publikováno v:
Vaccines, Vol 12, Iss 10, p 1094 (2024)
The South-East Asia (SEA) Region of the World Health Organization (WHO), through a Regional Committee resolution in 2013, adopted the goal of “measles elimination and rubella control by 2020”. The goal was revised in 2019 to “measles and rubell
Externí odkaz:
https://doaj.org/article/3a5a19a4b29a4679ad293be663bb109c
Autor:
Yahui Long, Kok Siong Ang, Mengwei Li, Kian Long Kelvin Chong, Raman Sethi, Chengwei Zhong, Hang Xu, Zhiwei Ong, Karishma Sachaphibulkij, Ao Chen, Li Zeng, Huazhu Fu, Min Wu, Lina Hsiu Kim Lim, Longqi Liu, Jinmiao Chen
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-19 (2023)
Advances in spatial transcriptomics technologies have enabled the gene expression profiling of tissues while retaining spatial context. Here the authors present GraphST, a graph self-supervised contrastive learning method that learns informative and
Externí odkaz:
https://doaj.org/article/64eff60cbac44eeaa66e55116960786f
Autor:
Mohammad Ahmad, Harish Verma, Abhishek Kunwar, Sudhir Soni, Ujjawal Sinha, Manish Gawande, Raman Sethi, Uma Nalavade, Deepa Sharma, Pankaj Bhatnagar, Sunil Bahl, Jagadish Deshpande
Publikováno v:
International Journal of Infectious Diseases, Vol 102, Iss , Pp 337-343 (2021)
Introduction: This study assessed the seroprevalence against all three polioviruses among the last cohort of infants aged 6-11 months who received tOPV before the tOPV-bOPV switch and had an opportunity to receive a full dose of inactivated polioviru
Externí odkaz:
https://doaj.org/article/2d5338f9bcaa4a0fa5aa6d1c0518310e
Autor:
Angeline Rouers, Ramapraba Appanna, Marion Chevrier, Josephine Lum, Mai Chan Lau, Lingqiao Tan, Thomas Loy, Alicia Tay, Raman Sethi, Durgalakshmi Sathiakumar, Kaval Kaur, Julia Böhme, Yee-Sin Leo, Laurent Renia, Shanshan W. Howland, Amit Singhal, Jinmiao Chen, Katja Fink
Publikováno v:
iScience, Vol 24, Iss 5, Pp 102482- (2021)
Summary: Clinically important broadly reactive B cells evolve during multiple infections, with B cells re-activated after secondary infection differing from B cells activated after a primary infection. Here we studied CD27highCD38high plasmablasts fr
Externí odkaz:
https://doaj.org/article/df7568f9beee4b21827039f78b71f536
Autor:
Gunadi, Fiko Ryantono, Raman Sethi, Marcellus, Alvin Santoso Kalim, Priscillia Imelda, Devy Melati, Susan Simanjaya, William Widitjiarso, Ririd Tri Pitaka, Nur Arfian, Kristy Iskandar, Akhmad Makhmudi, Poh San Lai
Publikováno v:
Journal of International Medical Research, Vol 49 (2021)
Objective Cluster genes, specifically the class 3 semaphorins ( SEMA3 ) including SEMA3C , have been associated with the development of Hirschsprung disease (HSCR) in Caucasian populations. We aimed to screen for rare and common variants in SEMA3C in
Externí odkaz:
https://doaj.org/article/596c8f4ebee44d14a781649e9086e53f
Autor:
Gunadi, Nova Yuli Prasetyo Budi, Raman Sethi, Aditya Rifqi Fauzi, Alvin Santoso Kalim, Taufik Indrawan, Kristy Iskandar, Akhmad Makhmudi, Indra Adrianto, Lai Poh San
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-9 (2018)
Abstract Background Hirschsprung disease (HSCR) is a heterogeneous genetic disorder characterized by absence of ganglion cells along the intestines resulting in functional bowel obstruction. Mutations in neuregulin 1 (NRG1) gene have been implicated
Externí odkaz:
https://doaj.org/article/fb94f85649cd429788fb49e748e91fda
Publikováno v:
PLoS ONE, Vol 12, Iss 6, p e0178776 (2017)
Retinoblastoma (RB) is a rare childhood malignant disorder caused by the biallelic inactivation of RB1 gene. Early diagnosis and identification of carriers of heritable RB1 mutations can improve disease outcome and management. In this study, mutation
Externí odkaz:
https://doaj.org/article/0f27909b47bf4fbd9a7e2fad5b3d1a1f
Autor:
Manoj V Murhekar, Mohammad Ahmad, Hemant Shukla, Kunwar Abhishek, Robert T Perry, Anindya S Bose, Rahul Shimpi, Arun Kumar, Kanagasabai Kaliaperumal, Raman Sethi, Vadivoo Selvaraj, Pattabi Kamaraj, Satyabrata Routray, Vidya Nand Das, Nata Menabde, Sunil Bahl
Publikováno v:
PLoS ONE, Vol 9, Iss 5, p e96668 (2014)
Updated estimates of measles case fatality rates (CFR) are critical for monitoring progress towards measles elimination goals. India accounted for 36% of total measles deaths occurred globally in 2011. We conducted a retrospective cohort study to est
Externí odkaz:
https://doaj.org/article/3e0653272f6d42b5bf5a3caf80f6858d