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RISHI BIOTECH
[ BIO-IT SERVICES & RESEARCH COMPANY ]
Bioinformatics [022-40120576,info@rishibiotech.com] :
Genomics :
- Biological sequence assembly and manipulation
- Genome annotation and analysis
- Biological sequence identification
- Gene finding and characterisation
- Comparative genomics: e.g. finding drug targets by comparing pathways from human and pathogen.
- Biological systems analysis
- Phylogenetic analysis (evolution of genes or proteins)
- Characterisation of gene regulatory elements
- Protein sequence annotation and characterization
- Microarray data analysis
- Drug Designing
- Rational Drug Design
We provide custom analysis to suit your requirement and services in a number of areas including:
- Automated Catalyst database updating standard
- Datasheet Catalyst massively parallel database building and searching
- Datasheet complete chemistry console
- Ensemble docking and scoring
- Grid integration for docking, scoring, and conformer generation
- ·Bisulfite Sequencing Service (Methyl-Seq)
- ·Bisulfite-based DNA methylation sequencing
- ·MeDIP Sequencing Service (MeDIP-Seq)
- ·MeDIP-based DNA methylation sequencing
- ·Methylation-Specific PCR
- ·Robust PCR for smaller scale DNA methylation analysis
- ·Global 5-mC Quantification
- ·ELISA-based assay for quantitation of total methylated cytosine levels in DNA
- ·hMeDIP Sequencing Service (hMeDIP-Seq)
- ·Multi-base resolution 5-hmC sequencing
- ·True 5-hmC Sequencing Service (Hydroxymethyl-Seq)
- ·Single base resolution 5-hmC sequencing
- ·Global 5-hmC Quantification
- ·ELISA-based assay for quantitation of total hydroxymethylated cytosine levels in DNA
- ·ChIP Sequencing Service (ChIP-Seq)
- ·Genome-wide chromatin immunoprecipitation sequencing
- ·ChIP Quantitative PCR Service (ChIP-qPCR)
- ·Robust quantitative PCR for smaller scale and affordable chromatin immunoprecipitation analysis
- ·ChIP Antibody Validation Service
- ·Validation of antibodies for successful use in ChIP-PCR, ChIP-on-chip, or ChIP-seq
- ·Epigenetic Analysis
- ·Sequencing & Expression Analysis
- ·De Novo Sequencing, Re-sequencing and Targeted Sequencing
- ·Genome Resequencing Data Analysis
- ·Identification of small structural variations (SVs) such as SNPs and DIPs;
- Identification of large SVs like deletions, insertions, duplications, inversions, genomic rearrangements, Copy Number Variations (CNV) and Presence Absence Variations (PAV);
- ·Genome consensus reconstruction;
- ·Genome Wide Association Studies (GWAS);
- ·High-throughput genotyping;
- ·Molecular evolution studies.
- ·Targeted & Exome Sequencing Data Analysis
- ·Identification of small structural variations (SVs) such as SNPs and DIPs;
- Identification of large SVs like deletions, insertions, duplications, inversions, genomic rearrangements, Copy Number Variations (CNV) and Presence Absence Variations (PAV);
- Genome Wide Association Studies (GWAS);
- High-throughput genotyping;
- High-throughput development of molecular markers;
- Molecular evolution studies
- Metagenomic Sequencing Data Analysis
- ·Analysis of species composition and abundance
- ·Genome components analysis
- ·Generate non-redundant gene catalog
- ·Gene functional annotations
- ·Comparative analysis among samples
- ·Transcriptomic Data Analysis
- ·Analysis Cases:
- ·Total RNA-Seq (Whole Transcriptome) Sequencing Data Analysis
- ·RNA-Seq (mRNA) Data Analysis
- ·Small RNA Resequencing Data Analysis
- ·With our de novo Sequencing Data Analysis service, we are able to provide:
- ·Identification of the expressed genes
- ·Identification of splicing variants
- ·Determination of the gene structures
- ·Quantification of absolute and relative gene expression levels
- ·Relative expression of different alleles
- ·SNP discovery and characterization
- ·Differential expression analysis
- ·Detection of post-transcriptional edits
- ·De novo RNA sequencing
- ·Identification of microRNAs including novel microRNAs
- ·Gene Ontology (GO) enrichment analysis
- ·Novel microRNA prediction
- ·Expression quantitation of known and novel microRNA
- ·Differential expression analysis of known and novel microRNA
- ·Target gene prediction and network/pathway analysis