It is estimated that the number of cancer cases worldwide will double by 2040. This makes the search for genes that cause cancer even more important. A team of researchers from the...
Read More »A component overlapping attribute clustering (COAC) algorithm for single-cell RNA sequencing data analysis and potential pathobiological implications
Recent advances in next-generation sequencing and computational technologies have enabled routine analysis of large-scale single-cell ribonucleic acid sequencing (scRNA-seq) data. However, scRNA-seq technologies have suffered from several technical challenges, including low mean expression levels...
Read More »RNA-Seq + machine learning may be able to predict if you’re in for a healthy old age
Doctors have long observed that biological age and chronological age are not always one and the same. A 55-year-old may exhibit many signs of old age...
Read More »FGMD – A novel approach for functional gene module detection in cancer
With the increasing availability of multi-dimensional biological datasets for the same samples (i.e., gene expression, microRNAs, copy numbers, mutations, methylations), it has now become possible to systematically understand the regulatory mechanisms operating in a cancer cell. For this task, it ...
Read More »Strawberry – Fast and accurate genome-guided transcript reconstruction and quantification from RNA-Seq
Iowa State University researchers propose a novel method and software tool, Strawberry, for transcript reconstruction and quantification from RNA-Seq data under the guidance of genome alignment and...
Read More »FreePSI – an alignment-free approach to estimating exon-inclusion ratios without a reference transcriptome
Alternative splicing plays an important role in many cellular processes of eukaryotic organisms. The exon-inclusion ratio, also known as percent spliced in, is often regarded as one of the most effective measures of alternative splicing events. The existing methods for ...
Read More »SQUID – Transcriptomic Structural Variation Detection from RNA-seq
Transcripts are frequently modified by structural variations, which leads to either a fused transcript of two genes (known as a fusion gene) or an insertion of intergenic sequence into a transcript. These modifications, called transcriptomic structural variants (TSV), can lead ...
Read More »ASAP – a Web-based platform for the analysis and interactive visualization of single-cell RNA-seq data
Single-cell RNA-sequencing (scRNA-seq) allows whole transcriptome profiling of thousands of individual cells, enabling the molecular exploration of tissues at the cellular level. Such analytical capacity is of great interest to many research groups in the world, yet these groups often ...
Read More »blkbox – Integration Of Multiple Machine Learning Approaches To Identify Disease Biomarkers
Machine learning (ML) is a powerful tool to create supervised models that can distinguish between classes and facilitate biomarker selection in high-dimensional datasets, including RNA Sequencing (RNA-Seq). However, it is variable as to which is the best performing ML algorithm(s) ...
Read More »MACAU – Differential Expression Analysis for RNAseq using Poisson Mixed Models
Identifying differentially expressed (DE) genes from RNA sequencing (RNAseq) studies is among the most common analyses in genomics. However, RNAseq DE analysis presents several statistical and computational challenges, including over-dispersed read counts and, in some settings, sample non-independence. Previous count-based ...
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