BLProt: prediction of bioluminescent proteins based on support vector machine and relieff feature selection

por Kandaswamy, Krishna Kumar, Pugalenthi, Ganesan, Hazrati, Mehrnaz Khodam, Kalies, Kai-Uwe, Martinetz, Thomas
Publicado em 2011

Insights into Protein Sequence and Structure-Derived Features Mediating 3D Domain Swapping Mechanism using Support Vector Machine Based Approach

por Shameer, Khader, Pugalenthi, Ganesan, Kandaswamy, Krishna Kumar, Suganthan, Ponnuthurai N., Archunan, Govindaraju, Sowdhamini, Ramanathan
Publicado em 2010

Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders

por Trinh, Joanne, Kandaswamy, Krishna Kumar, Werber, Martin, Weiss, Maximilian E. R., Oprea, Gabriela, Kishore, Shivendra, Lohmann, Katja, Rolfs, Arndt
Publicado no J Neurodev Disord (2019)

Homozygous Deletion of Exons 2 and 3 of NPC2 Associated with Niemann–Pick Disease Type C

por Hebbar, Malavika, Prasada L, Harsha, Bhowmik, Aneek Das, Trujillano, Daniel, Shukla, Anju, Chakraborti, Shrijeet, Kandaswamy, Krishna Kumar, Rolfs, Arndt, Kamath, Nutan, Dalal, Ashwin, Bielas, Stephanie, Girisha, Katta Mohan
Publicado no Am J Med Genet A (2016)

Development of an evidence-based algorithm that optimizes sensitivity and specificity in ES-based diagnostics of a clinically heterogeneous patient population

por Bauer, Peter, Kandaswamy, Krishna Kumar, Weiss, Maximilian E. R., Paknia, Omid, Werber, Martin, Bertoli-Avella, Aida M., Yüksel, Zafer, Bochinska, Malgorzata, Oprea, Gabriela E., Kishore, Shivendra, Weckesser, Volkmar, Karges, Ellen, Rolfs, Arndt
Publicado no Genet Med (2018)

Validation of a semiconductor next-generation sequencing assay for the clinical genetic screening of CFTR

por Trujillano, Daniel, Weiss, Maximilian E R, Köster, Julia, Papachristos, Efstathios B, Werber, Martin, Kandaswamy, Krishna Kumar, Marais, Anett, Eichler, Sabrina, Creed, Jenny, Baysal, Erol, Jaber, Iqbal Yousuf, Mehaney, Dina Ahmed, Farra, Chantal, Rolfs, Arndt
Publicado no Mol Genet Genomic Med (2015)

De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders

por Dulovic-Mahlow, Marija, Trinh, Joanne, Kandaswamy, Krishna Kumar, Braathen, Geir Julius, Di Donato, Nataliya, Rahikkala, Elisa, Beblo, Skadi, Werber, Martin, Krajka, Victor, Busk, Øyvind L., Baumann, Hauke, Al-Sannaa, Nouriya Abbas, Hinrichs, Frauke, Affan, Rabea, Navot, Nir, Al Balwi, Mohammed A., Oprea, Gabriela, Holla, Øystein L., Weiss, Maximilian E.R., Jamra, Rami A., Kahlert, Anne-Karin, Kishore, Shivendra, Tveten, Kristian, Vos, Melissa, Rolfs, Arndt, Lohmann, Katja
Publicado no Am J Hum Genet (2019)