Hi, is any perfect tool for analysis of whole genome sequence of bacteria?

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Is anyone familiar with DNA extraction from Manure ?

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CTAB capped silver nanoparticles to reduction 4-nitrophenol ?

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What is the successful procedure for synthesis core and shell quantum dots like CdSe/ZnS?

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hello,in Cisco packet tracer where can I find the data storage from the sensors in the figure?

hello, where can I find the data storage from the sensors in the figure?

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Hot press machine curing time?

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Are the frogs reproduce by parthenogenesis?

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How to correct the Rule of mixture?

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Which machine learning classifier will be used in numerous representation of Arabic corpus datasets. whether the accuracy rate has increased ?

Which machine learning classifier will be used in numerous representation of Arabic corpus datasets. whether the accuracy rate has increased compared to previous research techniques. ?

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Can I base on reverse DNA sequences to perform alignment, convert to amino acids and GenBank submission?

I have reverse sequences (AB1 format), can I base on reverse DNA sequences to perform nucleotide alignment, convert nucleotides to amino acids and deposit the sequence in GenBank database?

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How to confirm the site-directed mutagenesis result without performing NGS?

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Who of all the Global Scientific community will help me Prof. Dr. Yoshida make way for TPEOM, MEC ~EMC to return the atmospheric gases to the norma ?

TEP presentation caption (The Environmental Project) Re: Why should Washington’s DC, or any country government point of location think of as nowadays of as to being 'tomorrow as to come! if it...

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Does anyone have issues using Prepman Ultra reagent for MicroSeq ID bacterial, fungal and yeast sample preparation?

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How is the bacterial genome's high protein count verified as genuine despite 800+ contigs and good metrics (98.55%completeness, 0.68% contamination)?

Given that the bacterial genome has over 800 contigs, but its quality metrics are good, with a completeness of 98.55% and a contamination of 0.68% as assessed by CheckM, what specific validation...

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Recovery Viurses from bacteria genome?

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Should the amount of DNA input used for ChIP-seq library preparation be matched between the control and experimental groups?

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Can we convert a thousand of FASTA sequence in numeric form in .csv format? If yes kindly send me the script for the same?

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If my gene of interest has high GC content can it be problematic in sequencing? What kind of error is expected with GC rich gene sequences??

Gene sequencing related trouble shooting

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Can you visualize platelets using EVOS ?

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