Searching journal content for articles similar to Gettins 10 (12): 1833.

Displaying results 1-10 of 3574
For checked items
  1. OPEN ACCESS ARTICLE
  2. .... Using the ATAC-seq data, we developed a machine learning approach to determine the transcription factors (TFs) regulating the subtypes of GC. We identified TFs driving the mesenchymal (RUNX2, ZEB1, SNAI2, AP-1 dimer) and the epithelial (GATA4, GATA6, KLF5, HNF4A, FOXA2, GRHL2) states in GC. We...
  3. ...of nematodes is believed to date back to ∼650–750 million years, generating a large and phylogenetically diverse group to be explored. However, for most species high-quality gene annotations are incomprehensive or missing. Combining short-read RNA sequencing with mass spectrometry–based proteomics and machine...
  4. ...A somatic hypermutation–based machine learning model stratifies individuals with Crohn's disease and controls Modi Safra1,2,7, Lael Werner3,4,7, Ayelet Peres1,2, Pazit Polak1,2, Naomi Salamon5, Michael Schvimer6, Batia Weiss4,5, Iris Barshack4,6, Dror S. Shouval3,4,8 and Gur Yaari1,2,8 1The...
  5. ...technologies makes it possible to scrutinize the characteristics of cfDNA molecules, opening up the fields of cfDNA genetics, epigenetics, transcriptomics, and fragmentomics, providing a plethora of biomarkers. Machine learning (ML) and/or artificial intelligence (AI) technologies that are known...
    OPEN ACCESS ARTICLE
  6. ...Predicting unrecognized enhancer-mediated topology by an ensemble machine learning model Li Tang1,2, Matthew C. Hill3, Jun Wang4, Jianxin Wang1, James F. Martin2,3,5,6 and Min Li1 1Hunan Provincial Key Lab on Bioinformatics, School of Computer Science and Engineering, Central South University...
  7. ...research, from defining immune cell types by surface protein expression to defining diseases by their molecular drivers. Here, we describe a machine learning-based marker gene selection algorithm, NS-Forest version 2.0, which leverages the nonlinear attributes of random forest feature selection...
  8. ...not have consensus from multiple callers. Here, we present CN-Learn, a machine-learning framework that integrates calls from multiple CNV detection algorithms and learns to accurately identify true CNVs using caller-specific and genomic features from a small subset of validated CNVs. Using CNVs predicted...
  9. ....edu.cnAbstractPredicting phenotypes from genomic mutations remains a major genetic challenge. Traditional statistical methods (such as GBLUP and BayesR) have limitations, including reliance on artificial prior assumptions, and hard to capture epistatic effects. Machine learning (ML) has emerged as a powerful alternative for genomic...
  10. ...Laure Ciernik1,2,3,8, Agnieszka Kraft1,4,5,8,9,10, Florian Barkmann1, Josephine Yates1,4,6,11 and Valentina Boeva1,4,6,7 1ETH Zurich, Department of Computer Science, Institute for Machine Learning, 8092 Zurich, Switzerland; 2Machine Learning Group, Technische Universität Berlin, 10587 Berlin...
For checked items

Preprint Server