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

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

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

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

Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders

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

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

ανά 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
Τόπος έκδοσης 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

ανά 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
Τόπος έκδοσης Genet Med (2018)

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

ανά 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
Τόπος έκδοσης Mol Genet Genomic Med (2015)

De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders

ανά 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
Τόπος έκδοσης Am J Hum Genet (2019)