SAGE: a comprehensive resource of genetic variants integrating South Asian whole genomes and exomes

por Hariprakash, Judith Mary, Vellarikkal, Shamsudheen Karuthedath, Verma, Ankit, Ranawat, Anop Singh, Jayarajan, Rijith, Ravi, Rowmika, Kumar, Anoop, Dixit, Vishal, Sivadas, Ambily, Kashyap, Atul Kumar, Senthivel, Vigneshwar, Sehgal, Paras, Mahadevan, Vijayalakshmi, Scaria, Vinod, Sivasubbu, Sridhar
Publicado 2018

Whole genome sequencing identifies novel structural variant in a large Indian family affected with X-linked agammaglobulinemia

por Jain, Abhinav, Govindaraj, Geeta Madathil, Edavazhippurath, Athulya, Faisal, Nabeel, Bhoyar, Rahul C., Gupta, Vishu, Uppuluri, Ramya, Manakkad, Shiny Padinjare, Kashyap, Atul, Kumar, Anoop, Divakar, Mohit Kumar, Imran, Mohamed, Sawant, Sneha, Dalvi, Aparna, Chakyar, Krishnan, Madkaikar, Manisha, Raj, Revathi, Sivasubbu, Sridhar, Scaria, Vinod
Publicado 2021