}
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    • Tender For Sample Testing , Ngs Based Whole Genome Sequencing Of 15 Samples (Varieties And Nils) With 30 Gegabases Data For Each Sample And Identifying Polymorphism Thereof For Qtl Analysis : 1. Samples Will Be Picked Up From Bckv And Shipped To The, mohanpur-West Bengal

    Bidhan Chandra Krishi Viswavidyalaya has published Tender For Sample Testing , Ngs Based Whole Genome Sequencing Of 15 Samples (Varieties And Nils) With 30 Gegabases Data For Each Sample And Identifying Polymorphism Thereof For Qtl Analysis : 1. Samples Will Be Picked Up From Bckv And Shipped To The. Submission Date for this Tender is 17-03-2025. Laboratory Equipment Tenders in mohanpur West Bengal. Bidders can get complete Tender details and download the document.




    Tender Notice

    48115779
    Click Here To View Tendering Authority.
    Tender For Sample Testing , Ngs Based Whole Genome Sequencing Of 15 Samples (Varieties And Nils) With 30 Gegabases Data For Each Sample And Identifying Polymorphism Thereof For Qtl Analysis : 1. Samples Will Be Picked Up From Bckv And Shipped To The
    Open Tender
    Indian
    West Bengal
    Mohanpur
    17-03-2025

    Tender Details

    Sample Testing , Ngs Based Whole Genome Sequencing Of 15 Samples (Varieties And Nils) With 30 Gegabases Data For Each Sample And Identifying Polymorphism Thereof For Qtl Analysis : 1. Samples Will Be Picked Up From Bckv And Shipped To The Sequencing Firm On Dry Ice. If Required, Samples Will Be Picked Up Repeatedly Until The Quality Passes. 2. Qc Analysis Of Genomic Dna Using Gel Electrophoresis And Flurometer; Confirmation About Qc From Indenter Before Library Preparation. 3. Library Preparation Should Include Barcoded Library Preparation For (A) The Pacbio/Oxford Nanopore Platform And (B) The 150 Bp Pair-End (Pe) Library For The Illumina Novaseq Platform. 4.Sequencing—The Whole Genome Sequencing Work Must Deliver Both Long Reads (Using The Pacbio/Nanopore Sequencing Platform) And Short Read Data (Using The Illumina Novaseq Platform), Each With 15 Gegabases Of Data. 5. Bioinformatic Analysis Should Include Primary Read Statistics And Mapping Report, Sequence Qc (Fastqc/Multiqc) Results, De Novo Assembled Genome With Hybrid Reads, Chromosomal Assembly/Anchorage, Sequence Gap Polishing, Genome Annotations Including Gene And Repeat Elements, Gene Ontology, Pathway Analysis, Polymorphic Snps, In/Dels.And Their Use In Bulk Segregant Analysis. 6. Raw Sequencing Data Files Along With Analysis Report, And Supporting Files (Bamfiles) And Figures Should Be Shared Using Ssd Storage Device.

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