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How Our Genome Annotation Services Can Help You ?

RASA Bioinformatic Lab’s genome annotation services provides you a closer view on the genomic data analysis in understanding the data along with mapping, annotation and as well as comparative genome analysis of two different strains of same species, understanding its working de novo assembly of the genomic data and furthermore providing de-novo based RNA-Sequence Analysis of the data obtained. The impact of NGS technologies on genomics is far reaching and likely to change the field for years to come.

NGS technologies have demonstrated the capacity to sequence DNA at unprecedented speed, thereby enabling previously unimaginable scientific achievements and novel biological applications. Among which, genome annotation has remarkably gained the NGS applications, hence providing a huge area for genome annotation services for bioinformatics companies worldwide. But, the massive data produced by NGS also presents a significant challenge for data storage, analyses, and management solutions. RASA Bioinformatic CRO Lab’s  genome annotation services use advanced bioinformatics tools which are essential for the successful application of NGS technology. This results in striking impact on genomic research and the entire biological field including mapping, genome annotation and functional predictions along with comparative genomics analysis. Rasa Bioinformatic Lab’s  genome annotation services also enlighten the path towards its ability in tackling the unsolved challenges unconquered by previous genomic technologies.

 

Key Areas of Genome Annotation services

De-Novo Assembly

De novo assembly or sequencing refers to sequencing a novel genome where there is no reference sequence available for alignment. Sequence reads are assembled as contigs, and the coverage quality of de novo sequence data depends on the size and continuity of the contigs (ie, the number of gaps in the data). Next-generation sequencing (NGS) enables faster, more accurate characterization of any species compared to traditional methods, such as Sanger sequencing. Hence, genome assembly refers to the process of taking a large number of short DNA sequences and putting them back together to create a representation of the original chromosomes from which the DNA originated. Wherein, de novo genome assemblies assume no prior knowledge of the source DNA sequence length, layout or composition. In a genome sequencing project, the DNA of the target organism is broken up into millions of small pieces and read on a sequencing machine. These “reads” vary from 20 to 1000 nucleotide base pairs (bp) in length depending on the sequencing method used. RASA Bioinformatic Lab’s  genome annotation services can provide you a closer view on the de novo assembly and genome data analysis and furthermore providing de-novo based RNA-Sequence Data Analysis services for the obtained data.

 

Gene Mapping Service

Among the main goals of the Human Genome Project (HGP) was to develop new, better and cheaper tools to identify new genes and to understand their function. One of these tools is gene mapping. Genemapping also called linkage mapping can offer firm evidence that a disease transmitted from parent to child is linked to one or more genes. Gene Mapping also provides clues about which chromosome contains the gene and precisely where the gene lies on that chromosome.

Genetic maps are also useful in guiding scientists to the many genes that are believed to play a role in the development of more common disorders such as asthma, heart disease, diabetes, cancer, and psychiatric conditions. Identification of genes is usually the first step in understanding a genome of a species; mapping of the gene is usually the first step of identification of the gene. Gene mapping is usually the starting point of many important downstream studies. Hence we at RASA Bioinformatic CRO Lab’s genome annotation services can also perform gene mapping annotation to discover genes responsible for a disease or disorder or just to get data sufficient enough as the genetic counselling requirements, etc.

Our Publications

We have wide range of research publications which showcases the work we have carried out for different clients and our in-house R&D in the past few years.

Our Case Studies

Our service solutions apply to different purposes such as molecular medicine,microbial genome application,agriculture, animal,comparative studies,discoveries etc.

Genome Annotation Services Features

100% Post Service Assistance

We at RASA connect with our clients not only pre service or during service but also,after the service is delivered.

Data security

We assured highly secured data management and work environment.

Quality assurance

Our service aims at perfection and we deliver what is promised. We assure for quality assured services.

Experienced Team

Experienced portfolio management capabilities.

Service Customization

Apart from the package of services provided by us, we also customize service for our clients.

Free Services Training

We not only aim at delivering services but also provide onsite training on the services to the respective clients.

Our Achievements

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Our Genome Annotation Services Workflow

  • 1.

    Brainstorming

    Communicate your requirements along with your data and we will start working on the service.
  • 2.

    Design

    To finalize the steps required to successfully execute the service.
  • 3.

    Service Execution

    Start to work on the service keeping in mind the design & the data.
  • 4.

    Result Evaluation

    Generating results from the service & discussing the same so that client understand it thoroughly.

Clients' Testimonial

Meet Our Team

Our Key Areas Of Life Science's Services

Bioinformatics Consultancy Services

RASA experts help you to model 3D protein structures & identify opportunities to streamline your research with genomics & proteomic data analysis.

Next Generation Sequencing Data Analysis Services

RASA experts help you to manage, organize,analyze your any type of genomic data by using gold standard Next generation sequencing data analysis i.e NGS Data Analysis methods.

Computational Drug Discovery Services

RASA prowess in computational chemistry, structural biology, molecular modelling, simulation.

Customised Services

We at RASA understand that the research you do is innovative and novel. Innovative research needs innovative solutions.We do provide customization in our services according to your research requirement.

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We would love to assist you!Call at +917276010408 ,+919689904372

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