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Service Description
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Qty
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DNA sequencing single pass for Purified PCR product or plasmid DNA (500-600 bp sequence data from single-pass reaction using ABI BDT v3.1 Cycle Sequencing kit)
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Per reaction (For less than 100 samples)*
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DNA sequencing single pass for Purified PCR product or plasmid DNA (500-600 bp sequence data from single-pass reaction using ABI BDT v3.1 Cycle Sequencing kit)
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Per reaction (For less than 100 samples)
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PCR product purification and sequencing single pass reaction (500-600 bp sequence data from single-pass reaction using ABI BDT v3.1 Cycle Sequencing kit)
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Per reaction (For less than 100
samples)
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Plasmid DNA isolation from clones and DNA sequencing double pass (500-600 bp sequence data from each single pass reaction using ABI BDT v3.1 Cycle Sequencing kit)
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Per reaction (For less than 100
samples)
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Gel Elution of PCR product and DNA sequencing (500-600 bp sequence data from single-pass reaction using ABI BDT v3.1Cycle Sequencing kit)
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Per reaction (For less than 100
samples)
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PCR and sequencing (500-600 bp sequence data from single-pass reaction using ABI BDT v3.1 Cycle Sequencing kit)
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Per reaction (For less than 100
samples) Failed PCR will also be charged in full
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Sequence assembly (DNA sequence assembly using multiple overlapping fragments generated via primary walking; internal primer sequencing, contig sequencing; etc)
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Per sequence
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Manual Basecalling /Basecall editing (Basecalling and base editing, trimming of sequences using validated tools for final sequence confirmation, submission purposes)
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Per sequence
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Failed Sequencing reaction (A sequencing reaction that does not generate quality sequence data resulting a ‘Failed reaction’)
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Per reaction
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Conserved Gene Sequencing- 16S rDNA, 18S rDNA or ITS region (Using geneOmbio Primers) – deliverable only .ab1 sequences or sequence in FASTA format
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Per 500 bases In case the sample is mixed or contaminated culture sequence will be chimeric and will be charged the same
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Genomic DNA preparation from biological specimen – Yield of DNA up to 5 micrograms. Yield may vary based on specimen type
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Per sample
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Optimization of PCR for gene-specific amplification – For SNPs, microsatellites, homologous or novel genes
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Per Gene
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Adaptor ligation-mediated PCR and gene sequencing (Design of anchored adaptors, primers, PCR optimization, and gene sequencing)
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Per Gene
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