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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
 


