Our response time is short. We cope with the full range of bioinformatics job complexities. From simple over-night jobs through complicated tasks requiring a dedicated computational pipelines and even tasks which are not yet well-defined.
Computational process is carefully documented. End results are delivered in a methodical clear report, accompanied by graphs and heat-maps as required for the task. Service is offered at a cost-effective price and payment terms are flexible.
Bioinformatics-services is an enterprise led by Jonathan Monin, M.Sc. Physics, B.Sc. Mathematics, MBA and extensive experience in leading multi-disciplinary technological and scientific projects.
Expertise drawn from hands-on university and medical research projects and Bioinformatics algorithms courses.
Programming infrastructure - both Linux and Windows, R statistical environment, Python and C as required for optimizing memory and CPU time.
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Analysis launched on a set of NGS FASTQ files and included data filtering and trimming, read merging, overlap type of alignment, variants SNP detection and counting, characterization in hotspot and regional domains, creation of lineage trees and quantification of mutation rates. Use of IGMT database and UCSC genome browser.
Quality control is applied to FASTQ files, followed by mapping to the genome or directly to the transcriptome. De-duplication of UMI is applied, case dependent. Producing TPM and count tables. Clustering analysis: dendrograms, correlation matrices, PCA and tSNE. Differential Gene (DE) analysis using either classic tools (e.g. DESEq2) or custom workflows. Selection of genes based on fold-change and p-values. Interpretation of the results by comparison with pathway and GO gene sets.
Input data in the form of CEL files resulting from probe-based micro-arrays. Noise reduction and normalization to obtain differential expressions across all genes. Performing both gene ontology (GO) enrichment analysis and mapping against Kyoto's KEGG database. Establishing timeline expression heatmaps across samples. An RNAseq computational pipeline is set for projects requiring deeper resolutions at the exon and isoform levels.
Several different epigenomic-related projects: starting from methylation array data (e.g. HumanMethylation450 beadchip array or bisulfite sequencing files) and identifying unique pattern and regional characteristics accompanied by phenotype correlation against control or databases (e.g. TCGA database - Cancer Genome Atlas) all for different medical research projects.
Reference-based global, local and overlap alignments, whole-genome short-read alignments, bisulfite sequencing alignment (agnostic to CpG sites), RNAseq alignments (cross exon-junctions) and BLAST tools. Exploring parametric effects on alignment outcomes.