Convert a FASTA sequence into multiple sequences
Paste FASTA sequences. Input limit is 500,000,000 characters.
The length of each new sequence fragment in bases.
The number of bases to overlap between consecutive fragments (0 for no overlap).
Paste your FASTA sequences. The tool accepts DNA, RNA, or protein sequences and automatically removes formatting characters.
Specify the desired fragment length and overlap. Use overlap of 0 for non-overlapping fragments, or set a value for sliding window analysis.
Run the tool to split sequences into fragments. Each fragment is labeled with its position range and includes metadata in the FASTA header.
Save the fragmented sequences for sliding window analysis, parallel processing, k-mer studies, or assembly simulation.
Create overlapping fragments for sliding window analysis of sequence features, GC content, or motif distribution.
Split long sequences into manageable fragments for parallel processing or analysis with tools that have length limits.
Generate overlapping k-mers or fixed-length subsequences for pattern recognition and sequence comparison.
Create overlapping reads to simulate sequencing data or test assembly algorithms.
Example 1: No Overlap
ABCDEFGHIJ (10 bases)ABC (positions 1-3)DEF (positions 4-6)GHI (positions 7-9)J (positions 10-10)Example 2: With Overlap
ABCDEFGHIJ (10 bases)ABCD (positions 1-4)CDEF (positions 3-6) ← overlaps by 2EFGH (positions 5-8) ← overlaps by 2GHIJ (positions 7-10) ← overlaps by 2Each fragment is output as a FASTA record with a descriptive header:
>fragment_N;original_title_start=X;end=Y;length=Z;source_length=T