Sequencing Analysis Services

NGS Based sequencing BRCA 1 and BRCA 2 Gene Sequencing by Discovery scientific , kotturpuram, chennai.

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Enhance your microbial research with our advanced nanopore sequencing services. We offer high-resolution sequencing for detailed microbial genome insights, rapid turnaround times, and comprehensive data analysis. Our custom solutions are tailored to meet your specific research needs, supported by our team of experienced scientists. Applications: Microbial diversity studies Pathogen detection Antibiotic resistance research Metagenomics Trust our cutting-edge technology and expert support to deliver reliable and impactful results for your microbial studies.

1.(a) 16S rDNA sequencing of Bacteria / Actinomycetes (from pure culture) Rs. 5,500/- (b) 16Sr DNA Gene sequencing for Bacterial identification, the whole up to 1500-bp length Rs. 8,500/- (c) 16Sr RNA Sequencing Rs. 9000/- 2.(a) 18S rDNA sequencing of Fungi / Yeast (from Pure Culture) Rs 10,000/- (b) 18Sr DNA Gene sequencing for Fungi / Yeast identification, the whole up to 1500-bp length Rs.13,000/- (c) 18Sr RNA Sequencing Rs. 9000/-

The 3326 Next Genetic Sequence Cryostat Microtome is an advanced instrument for rapid pathology testing, offering precise tissue sectioning with high efficiency. It features a large touchscreen interface, dual German Danfoss compressors, UV sterilization, and a fully enclosed freezing chamber for enhanced safety and cleanliness. Suitable for histology labs and research applications requiring high-quality, thin tissue slices. Key Features: Section thickness range: 0.5 m 100 m adjustable. Horizontal stroke: 22 mm; Vertical stroke: 65 mm. Dual Danfoss compressors for separate chamber and blade cooling. 24-position freezing shelf with semiconductor refrigeration. Fast cooling to -60 C within 15 minutes. UV sterilization and waste collection system. LCD display with intuitive controls. Safety handwheel lock and 360 arbitrary point locking.

Testing your cancer genes will help in detecting hereditary cancer diseases early in order to find certainty, identify risks, and start timely treatment.With myLifeCancer , we sequence your entire genomic DNA and analyse more than 1300 genes related to cancer. After every analysis, you will receive a detailed report with further information and action points. myLifeCancer also includes a subscription to quarterly updates of your results based on most recent scientific knowledge.Highest-quality interpretation of your genomic dataAnalysis of more than 1300 cancer genes based on your symptomsQuarterly updated results based on scientific knowledgeAccess to professional genomic counselingSamplingKit and global free shipping included Regular updates Quarterly updates of your genomic results based on the most recent scientific knowledge. Incidental findings With your consent we report previously unknown genomic results in specific genes that have a treatment consequence but are not related to your potential clinical symptoms. Easy to understand Results and recommendations are presented in a suitable way for non-medical people and more in-depth for genomic experts.

We Do gene targetting of 16S rRNA gene of bacterium by PCR followed by Sequencing and Bioinformatics studies and lastly gives facility for accesssion number

16S and ITS rRNA sequencing are popular methods for identifying and comparing bacteria or fungi in samples. The 16S rRNA gene in prokaryotes is about 1500 bp long, featuring nine variable regions among conserved ones. These variable regions are often employed to classify genus or species in various microbial populations. The ITS1 region of the rRNA cistron serves as a common DNA marker for pinpointing fungal species in metagenomic samples.

To cater the variegated demands of our precious clients, we are highly engrossed in providing a qualitative DNA Sequencing Services. This service is carried out under the supervision of our experts who maintain all the quality standards prescribed by leading industry. To cater this service, our highly experienced professionals use the best quality tools and high-end technology. Moreover, the offered service is highly reliable and carried out in compliance with the set quality standards.

We are the best service provider of Microbial Identification Service. Accurate identification of bacterial isolate is very important for researchers. Identification of many organisms by traditional phenotypic method may be difficult, laborious and time consuming. Today taxonomists consider analysis of an organism's 16S rRNA gene (16S rDNA) which found in all bacteria and archaea more reliable than phenotypes. The 16S rRNA gene is codes for ribosomal rRNA and this in turn makes up part of the small subunit (SSU) of prokaryotic ribosome. The length of rRNA gene is approximately 1500bp and has conserved regions as well as hypervariable regions containing species specific signature sequences useful for bacterial identification to species level.

Shotgun metagenomic sequencing is a relatively new environmental sequencing approach used to examine thousands of organisms in parallel and comprehensively sample all genes, providing insight into community biodiversity and function. Shotgun sequencing allows for the detection of low abundance members of microbial communities. Shotgun metagenomics methods are enabling a deeper analysis of the gut microbiome and how it contributes to, or protects from, disease.

We offer advanced genotyping services to help researchers, healthcare providers, and industries gain deeper insights into genetic information. Our state-of-the-art technologies and expertise allow us to provide reliable genetic analysis for a variety of applications, including research, diagnostics, and personalized medicine.

To identify bacterial species using a sample, scientists commonly utilize 16S rRNA gene sequencing which involves extracting and amplifying a specific region of the 16S rRNA gene from the bacterial DNA, then comparing the sequence to a database of known bacterial 16S rRNA sequences to determine the most likely species based on its unique variable regions within the gene; this method allows for identification of bacteria even from complex samples where multiple species may be present.

Targets 139 amplicon regions of 16 genes, including AKT1, BAP1, BRCA1, BRCA2, BRIP1, CCND1, CHEK2, EP300, ERBB2, GATA3, MAP2K4, PALB2, PBRM1, PIK3CA, RB1, and TP53. (CE-IVD)

Next Generation Sequencing (NGS) Analysis Service:Comprehensive and high-throughput sequencing data analysis for genomics, transcriptomics, and metagenomics studies. Our service delivers accurate insights into genetic variation, gene expression, microbial diversity, and more supporting research, diagnostics, and precision medicine. Key Features: Whole Genome, Exome Transcriptome Analysis Variant Calling, Annotation Interpretation RNA-Seq, miRNA-Seq Epigenetic Analysis Microbiome Metagenomic Profiling Custom Bioinformatics Pipelines tailored to project needs Publication-Ready Reports Visualizations Secure Data Handling and expert consultation

Oxford Nanopore Sequencer to your laboratory Genotypic, India's pioneer in genomics is appointed as the FIRST distributor for Oxford Nanopore Technologies in India. Applications Genome Scaffolding,Metagenomics, MethylationProfiling, Direct RNA Sequencing,Fusions and Splice Variants Domains Medical Microbiology, Vaccines, Biopharma, Basic Research Direct DNA/RNA sequencingREAL Real-timeLow capital cost requiredUltra-long readsScalable to portable or desktop10 min library prepHigh-fidelityHigh yields for large genomes

Children arrange each set in logical order and tell the story in their own language.Ages: 3 & up Children arrange each set in the proper order\sequence and tell the story in their own language. Children understand how events have a beginning and an end and suggest suitable titles for the stories/events.

Whole Exome Sequencing is gaining popularity as a viable and cost-effective alternative for Whole Genome Sequencing. We have performed professional sequencing services for many years at multiple locations globally, to support biomedical research and to benefit small and large-scale clinical trials and other projects in pharmaceutical drug development. Whole Exome Sequencing services are executed with the Illumina HiSeq 4000 sequencing system. Sample Preparation and Services 100bp and 150bp paired-end sequencing options availableAgilent Sureselect, NimbleGen SeqCap or KAPA Hyper Prep kit for library construction and enrichmentRaw data and bioinformatics analysis are available in standard file formatsAdvanced and custom bioinformatics data analysis availableCloud-based data storage and delivery systemSequencing Quality Standard Guaranteed 80% of bases with quality score of Q30Standard sequencing coverage 50X; 150X is recommended for cancer samplesTurn Around Time Typical 40 working days from sample QC acceptance to filtered raw data availability.Expedited services are available, contact your local specialist for details

Sanger Sequencing Fragment Analysis By CE is used to study a small subset of genes linked to a defined phenotype, confirm next-generation sequencing (NGS) variants, detect minor allele fractions down to 5%, or read contiguous sequences up to 1,000 bases. Fragment analysis is a powerful technique with simple, straightforward workflows and used in a wide-range of applications, such as detection of mutations, genotyping, identification of short tandem repeats, and gene expression profiling. Applied Biosystems genetic analysis systems are a trusted standard for Sanger sequencing and fragment analysis by capillary electrophoresis proven through decades of results, including the first sequencing of the human genome and the discovery of genes implicated in diseases like cystic fibrosis. Explore applications, instrumentation, reagents, consumables, and software designed to respond to the unlimited potential of scientific inquiry.

The ViroSeq HIV-1 Genotyping System is intended for use in detecting HIV genomic mutations that confer resistance to specific types of antiretroviral drugs, as an aid in monitoring and treating HIV infection. Specifically, the ViroSeq HIV-1 Genotyping System can be used to: Detect HIV-1 Subtype B viral resistance in plasma samples collected in EDTA with a viral load ranging from 2000 to 750,000 copies/mL Genotype the entire HIV-1 protease gene from codons 1-99 and two-thirds of the reverse transcriptase (RT) gene from codons 1-335 Features: The indications for use encompass the following populations:HIV-1 infected individuals at drug therapy failure (with increased viral load) before therapy switchHIV-1 infected individuals at initial presentation, before initial drug therapy

Sequence data analysis (Basic and Advanced) - Phylogenetic analysis - Application of pattern recognition tools on sequence data to derive signatures. - New algorithm development, statistical analysis of sequence data generated on varied platforms like 454, Solexa and SOLiD. - Assembly of Next-Gen sequence data, annotation and classification of sequence data. - Differential expression analysis based on copy number data. - Meta-genome data management and analysis.

WES is conventionally recommended when patients present complex, heterogeneousphenotypes that are suggestive of multiple conditions or are otherwise unclear or atypical.WES may also be recommended when a prior genetic test was unsuccessful. The latest clinical evidence also supports WES as a first-line test when a patient s symptoms or family history suggests a genetic cause of the diseases. This is especially true for neurodevelopmental disorders, including intellectual disability, global developmental delay, and autism spectrum disorder due to the high diagnostic yield. The test results from WES may also lead to more rapid diagnoses, improved prevention of symptomatic illness, more targeted treatments or even end the need for some costly or invasive procedures.

ProGenome Life Science Pvt Ltd. offers cutting-edge Metagenomics Next Generation Sequence (NGS) Services, providing comprehensive insights into the genetic composition, functional potential, and ecological dynamics of microbial communities in diverse environments. Metagenomics harnesses high-throughput sequencing technology to analyze DNA samples directly extracted from environmental samples, enabling researchers to explore the vast microbial diversity and functionality without the need for microbial culturing. Our metagenomics services support a wide range of applications in environmental microbiology, biotechnology, clinical diagnostics, and beyond Metagenomics NGS involves the sequencing of DNA fragments from complex microbial communities present in environmental samples such as soil, water, air, and host-associated microbiomes. Unlike traditional microbiological approaches that rely on isolating and culturing individual microbial species, metagenomics allows for the simultaneous analysis of all microorganisms present in a sample, providing a holistic view of microbial diversity, functional potential, and community interactions. ProGenome Life Science Pvt Ltd. is your premier partner for Metagenomics Next Generation Sequence Services, delivering comprehensive insights into microbial communities and their functional potential across diverse environments and applications. Our state-of-the-art technology, expert team, and customized solutions empower researchers to unlock the mysteries of microbial diversity, ecology, and biotechnological innovation.

NGS sequencing with data interpretation with bioinformatics expert.

We are engaged in offering a qualitative Next Generation Sequencing Service to our valuable clients. We offer this service in an excellent manner within a scheduled time-frame. The offered service is performed by our highly qualified professionals using excellent grade tools and advanced technology. Owing to its perfect execution and flawlessness, this service is widely appreciated by our precious clients. Further, we provide this service as per the requirements of our clients at most affordable price.

BioEdge Solutions offer all kinds of services related to Biotechnology and stands to be one of the standard service provider. The research team always welcome queries relating to potential evaluation of experiments to fulfill their customers. We wholeheartedly encourage the association with life sciences companies, universities, academic institutions, eminent scientists and other members. Below links supplement our business stream and technical expertise.

V3-V4 Bacterial Metagenomics

DNA Sanger Sequencing