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DNA Sequencing Services
DNA Sequencing Services
Flexibility and expertise are the key features of our sequencing service.
Our scientists have more experience in delivering large and small scale sequencing projects providing both traditional Sanger sequencing and Next Generation Sequencing (NGS) services to a global customer base. Expertise includes collaborations in a variety of national and international genome projects.
We offer full bioinformatics support and can assist with project design, provide advice on difficult targets and genomes and assist in the generation of a service proposal that drives maximum benefit and cost-effectiveness.
As a provider of services across the genomics value chain we understand the importance of your data, its interpretation and can help with the next stage of your research.
Sanger Sequencing
Sanger Sequencing
- High-throughput sequencing including - MTP (microtiter plate) in 96 well format
- Re-sequencing of genes and or genomic regions
- Single read sequencing
- Primer walking projects
- Primer design and synthesis
- DNA isolation including large constructs
- Cloning of PCR products or DNA fragments
- PCR amplification and / or purification
- Library services (normalised cDNA, cosmid / fosmid, shotgun)
- Microbial identification
- Bacterial pure culture (16S rDNA)
- Fungal pure culture (18S or ITS rDNA)
- Yeast pure culture (18S or ITS rDNA)
- Qualitative identification in complex samples.
NGS Sequencing
NGS Sequencing
- De novo sequencing
- Exome (Targeted) Re-sequencing of genomes
- Transcriptome sequencing and analysis (of both eukaryotic and prokaryotic organisms)
- Metagenome sequencing and analysis
- Analysis of:amplicons (e.g. 16S rDNA)
- Genotyping in Thousands by sequencing (GT Seq)
- Bisulfite sequencing
- Small RNA sequencing
- Chip Sequencing
- RAD sequencing
Contact our sequencing team.
Contact our sequencing team.
Phone: +91 836-2449444
Email: clovergenls@gmail.com
Genotyping by Sequencing (GBS)
Genotyping by Sequencing (GBS)
Genotyping by Sequencing (GBS) is the cost effective method of choice for genome wide SNP discovery without prior knowledge of the genome sequence.
Applications
Applications
Applications for genotyping by sequencing include:
- Co-dominant SNP Genotyping
- Genetic Diversity Analysis
- Genetic Mapping
- QTL Mapping
- Bulk Segregant Analysis
- Mapping to Whole Genome Sequence
- Discovery of (rare) SNP variants
- Genome Wide Association Mapping
- Genomic Selection/Prediction
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