What We Do
- Map, analyse and report variations within the genome
- Send a complete report within 7 days upon receipt of data
- Apply pipelines to other organisms, where reference genomes are available
Accelerating Your Journey of Discovery
Sequence. Analyse. Innovate.
Sequence. Analyse. Innovate.
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Contract Genomics Services
Our comprehensive range of cutting-edge sequence analysis pipelines is designed to cater for the specific project requirements of our customers. These proprietary pipelines are built to rank, filter and analyse reads from all major next-generation sequencing platforms. Customers can save on time and cost, and focus on publishing their results more rapidly.
Through this service, the genome is analysed for variations. Known and novel sequence polymorphisms, insertions, deletions and large-scale genomic re-arrangements are characterised for subsequent downstream analysis.
What We Do
What We Do
Genes are identified using DNA sequence information and are then assigned with names, keywords and putative functions through functional analysis. Similarities between genomes are also characterised using comparative genomics.
What We Do
What We Do
- Predict and identify structural genes and RNAs on the genome
- Identify and classify functional genes
- Provide comparative genomics and genome sequence analysis
- Produce a comprehensive report on annotation
Raw reads are analysed, and only high quality ones are channelled into pipelines.
What We Do
What We Do
- Pre-process raw reads and remove contamination
- Filter low quality reads
- Produce detailed pre-process report containing raw read summary and read quality statistics
Our pipelines are designed to provide a view of known and novel single nucleotide variants (SNVs) within the exons in the genome. Detailed information on alternative splicing, gene expression levels and SNVs within the transcriptome is also reported.
What We Do
What We Do
- Assemble exomes and transcriptomes de novo
- Map exome and transcriptome reads to reference mRNA
- Provide statistical gene expression analysis
- Identify copy number variation (CNV) and SNVs in exomes and transcriptomes
De novo assembly and scaffolding of genomes of various sizes and complexities are provided using paired-end reads from next-generation sequencing experiments. Genomes are also assembled based on known or highly homologous reference genomes.
What We Do
What We Do
- Map transcriptome reads to an assembled genome for validation purposes
- Provide a detailed report on assembly statistics
- Customise output based on customer requirements and objectives of research
Other analytical pipelines include workflows for the handling of ChIP-Seq data, microRNA annotation and analysis, and further mutation analysis. Also offered are consultation on emerging bioinformatics technologies and customised services.
Human Genome Offer
Genome Bioinformatics Services (delivered within 7 days)
Additional Services
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