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

par Kandaswamy, Krishna Kumar, Pugalenthi, Ganesan, Hazrati, Mehrnaz Khodam, Kalies, Kai-Uwe, Martinetz, Thomas
Publié 2011

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

par Shameer, Khader, Pugalenthi, Ganesan, Kandaswamy, Krishna Kumar, Suganthan, Ponnuthurai N., Archunan, Govindaraju, Sowdhamini, Ramanathan
Publié 2010

Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders

par Trinh, Joanne, Kandaswamy, Krishna Kumar, Werber, Martin, Weiss, Maximilian E. R., Oprea, Gabriela, Kishore, Shivendra, Lohmann, Katja, Rolfs, Arndt
Publié dans J Neurodev Disord (2019)

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

par 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
Publié dans 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

par 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
Publié dans Genet Med (2018)

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

par 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
Publié dans Mol Genet Genomic Med (2015)

De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders

par 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
Publié dans Am J Hum Genet (2019)