How to remove low quality reads?

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Are you looking for research collaboration ?

we have few papers ready for submission, and we need one co-author for each article who can pay article fee. Interested authors may text here or contact me on my following email id [email protected]

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Dear researchers. pl help how to plot jablonski energy level graph and magnetic hysteresis curve in origin?

through origin software

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What is the acceptable p-value cutoff for GO enrichment analysis ?

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Inquiry on Maximum Nucleic Acid Volume for 2.5 mL Liposome Solution?

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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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Optimal siRNA Volume for Complexation with Liposomes in a 2.5 mL Solution with 10 mg/mL Lipid Concentration?

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Joshua Beytebiere

There is a question similar to this one located here:

https://www.researchgate.net/post/Can_anyone_explain_to_me_how_to_filter_low-quality_reads_and_the_principle_behind_including

Should be able to answer your question.

Abhijeet Singh

Cutadapt or Trimmomatic

Both software can be used for both primer trimmer and quality filtering

Wiwiek Harsonowati

I am using SnapGene or ChromasPro

Michael Ackah

Using FastQC tool will help as wll

Are you sure you have correct understanding about what you are suggesting...

Or can you describe how the task in the question can be achieved by the tool you suggested?