Trim adapters, remove low-quality bases, and clean sequences for downstream NGS analysis
Sequence trimming removes unwanted bases from sequencing reads to improve data quality. This includes removing adapter sequences added during library preparation, trimming low-quality ends, removing primers, and filtering sequences that don't meet quality standards. Essential preprocessing step for NGS analysis.
Follow these steps:
This tool is useful when you need to:
Sequences with adapters and low-quality ends:
>Read1
AGATCGGAAGAGCACACGTCTGAACTCCAGTCACATCACGATCTCGTATGCCGTCTTCTGCTTGAAA
>Read2
NNNGATCGTAGCTAGCTAGCTAGCTAGNNN Adapter: AGATCGGAAG, Low quality N's present
Cleaned sequences after trimming:
>Read1
GCACACGTCTGAACTCCAGTCACATCACGATCTCGTATGCCGTCTTCTGCTTGAAA Read2 removed (contains N's), adapter trimmed from Read1.
Q: What adapters are auto-detected?
A: Illumina TruSeq (AGATCGGAAG), Nextera (CTGTCTCTTATACACATCT), and common primers.
Q: Should I trim before or after quality filtering?
A: Typically trim adapters first, then filter by quality and length.
Q: What is a good minimum length?
A: For short reads: 20-30bp. For long reads: 50-100bp. Depends on downstream analysis.