Results 51 to 60 of about 3,559,306 (120)

Software Measurement for Functional Programming [PDF]

This thesis presents an investigation into the usefulness of software measurement techniques, also known as software metrics, for software written in functional programming languages such as Haskell.
Ryder, Chris
core  

Comprehensive evaluation of structural variation detection for germline and somatic analysis with long-read sequencing data. [PDF]

Brief Bioinform
Shi H, Lin Y, Liu D, Wu H, Mat Isa AN, Wei L, Zou Q, Chen X.   +7 more
europepmc   +1 more source

Deep learning detection of retinitis pigmentosa inheritance forms through synthetic data expansion of a rare disease dataset. [PDF]

Sci Rep
Hwang EE, Rivera ML, Lin MT, Zéboulon P, Nachnani K, Yuan O, Madaan P, Han Y, Duncan JL, Jia L, Shan J.   +10 more
europepmc   +1 more source

From Traditional Inspection to Quantitative Imaging: Tongue and Facial Color Features for Automated Machine Learning-Driven Depression and Schizophrenia Classification. [PDF]

Behav Sci (Basel)
Gao L, Zhang M, Li Y, Wang L, Qian P, Tong J, Fu H, Sun X, Li F.   +8 more
europepmc   +1 more source

Decomposition of Inheritance Hierarchy DAGs for Object-Oriented Software Metrics

, 2010
[[abstract]]Software metrics are widely used to measure software complexity and assure software quality. However, research in the field of software complexity measurement of a class hierarchy has not yet been carefully studied.
Timothy K. Shih; Chi-Ming Chung; Chun-Chia Wang; Wen C. Pai
core  

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women. [PDF]

Ann Med
Hu L, Cao X, Zeng S, Wen L, Zhong J, Liu Y, Liu W, Wei F.   +7 more
europepmc   +1 more source

DAQ-YOLO:a high precision counting model for maize seedlings in dense scenes. [PDF]

Front Plant Sci
He X, Wang H, Ma Z, Li K, Zhou T, Liu Y, Zhou Y, Zhang X.   +7 more
europepmc   +1 more source

The spectrum of copy number variation in the Pan-Canadian HostSeq databank. [PDF]

PLoS One
Aujla N, Thiruvahindrapuram B, Casalino S, Frangione E, Mahajan R, Di Iorio D, Fung CYJ, Jayachandran L, MacDonald G, Morgan G, Wolday D, Young J, Arshad M, Clausen M, Arnoldo S, Binnie A, Borgundvaag B, Chowdhary S, Dagher M, Devine L, Friedman SM, Gingras AC, Goneau LW, Khan Z, Lapadula E, Mazzulli T, McGeer A, McLeod S, Mighton C, Pugh TJ, Richardson D, Simpson J, Stern S, Taher A, Strug L, Bombard Y, Faghfoury H, Greenfeld E, CGEn HostSeq Initiative, Scherer SW, Taher J, Noor A, Lerner-Ellis J.   +42 more
europepmc   +1 more source

Integration of Machine Learning-Based Pathogenicity Prediction and Phenotype Matching Improves Variant Prioritization in Rare Clinical Testing. [PDF]

Curr Issues Mol Biol
Ruzicka J, Ravel JM, Audoux J, Boulat A, Thévenon J, Yauy K, Dancer M, Raymond L, Lombardi Y, Philippe N, Blum MG, Duforet-Frebourg N, Mesnard L.   +12 more
europepmc   +1 more source

Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 families. [PDF]

Orphanet J Rare Dis
Davarzani A, Ravanbod M, Ghasemi A, Mohammadi M, Rohani M, Nafissi S, Jamali P, Najmabadi H, Fatehi F, Alavi S, Firoozfar Z, Zemorshidi F, Habibi-Kavashkohie MR, Alavi A.   +13 more
europepmc   +1 more source