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Yan W. Asmann
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2020 – today
- 2022
- [j10]Yongbing Zhao
, Jinfeng Shao
Assessment and Optimization of Explainable Machine Learning Models Applied to Transcriptomic Data. Genom. Proteom. Bioinform. 20(5): 899-911 (2022) - 2020
- [j9]Pramod Chandrashekar
Somatic selection distinguishes oncogenes and tumor suppressor genes. Bioinform. 36(6): 1712-1717 (2020)
2010 – 2019
- 2019
- [j8]Yongbing Zhao
NucMap: a database of genome-wide nucleosome positioning map across species. Nucleic Acids Res. 47(Database-Issue): D163-D169 (2019) - 2018
- [j7]Yingxue Ren, Joseph S. Reddy, Cyril Pottier
Identification of missing variants by combining multiple analytic pipelines. BMC Bioinform. 19(1): 139:1-139:12 (2018) - 2014
- [j6]Chen Wang
PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data. Bioinform. 30(18): 2678-2680 (2014) - [j5]Chen Wang
RVboost: RNA-seq variants prioritization using a boosting method. Bioinform. 30(23): 3414-3416 (2014) - [j4]Krishna R. Kalari
MAP-RSeq: Mayo Analysis Pipeline for RNA sequencing. BMC Bioinform. 15: 224 (2014) - 2012
- [j3]Yan W. Asmann, Sumit Middha
TREAT: a bioinformatics tool for variant annotations and visualizations in targeted and exome sequencing data. Bioinform. 28(2): 277-278 (2012) - [j2]Zhifu Sun
SAAP-RRBS: streamlined analysis and annotation pipeline for reduced representation bisulfite sequencing. Bioinform. 28(16): 2180-2181 (2012)
2000 – 2009
- 2009
- [j1]High-Seng Chai, Hugues Sicotte, Kent R. Bailey, Stephen T. Turner, Yan W. Asmann, Jean-Pierre A. Kocher:
GLOSSI: a method to assess the association of genetic loci-sets with complex diseases. BMC Bioinform. 10 (2009)
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