Multi omics analysis of fibrotic kidneys in two mouse models.
miRNA variants (isomiRs): real molecules or sequencing artifacts?
MiRNA Wars: The isomiRs menance
Unification of miRNA and isomiR research: the mirGFF3 format and the mirtop API
miRTOP: An open source community project for the development of a unified format file for miRNA data
Circulating miRNAs, isomiRs and small RNA clusters in human plasma and breast milk
bcbioRNASeq: R package for bcbio RNA-seq analysis
Maintenance of macrophage transcriptional programs and intestinal homeostasis by epigenetic reader SP140
Molecular, phenotypic, and sample-associated data to describe pluripotent stem cell lines and derivatives
Empirical comparison of reduced representation bisulfite sequencing and Infinium BeadChip reproducibility and coverage of DNA methylation in humans
Characterization of the small RNA transcriptome using the bcbio-nextgen python framework
Specific small-RNA signatures in the amygdala at premotor and motor stages of Parkinson's disease revealed by deep sequencing analysis.
The small RNA content of human sperm reveals pseudogene-derived piRNAs complementary to protein-coding genes.
Functional Impact and Evolution of a Novel Human Polymorphic Inversion That Disrupts a Gene and Creates a Fusion Transcript
Paternal Diet Defines Offspring Chromatin State and Intergenerational Obesity
InvFEST, a database integrating information of polymorphic inversions in the human genome
A highly expressed miR-101 isomiR is a functional silencing small RNA.
Microarray and deep sequencing cross-platform analysis of the mirRNome and isomiR variation in response to epidermal growth factor.
A Pathogenic Mechanism in Huntington's Disease Involves Small CAG-Repeated RNAs with Neurotoxic Activity.
A non-biased framework for the annotation and classification of the non-miRNA small RNA transcriptome.
A myriad of miRNA variants in control and Huntington's disease brain regions detected by massively parallel sequencing
SeqBuster, a bioinformatic tool for the processing and analysis of small RNAs datasets, reveals ubiquitous miRNA modifications in human embryonic cells
Fibroblast-derived induced pluripotent stem cells show no common retroviral vector insertions.
Identification of Copy Number Variants Defining Genomic Differences among Major Human Groups
ProSeeK: A web server for MLPA probe design
Genome assembly comparison identifies structural variants in the human genome.