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Raw reads were cleaned by removing adaptor sequences.
The original reads were cleaned by removing adaptor sequences and short reads (reads of < 15 bp).
The raw reads were cleaned by removing adaptor sequences, duplicated reads and low quality reads.
The raw reads were cleaned by removing adaptor sequences, empty reads and low quality sequences.
For each sample, the raw reads were cleaned by removing adaptor sequences in two steps.
The raw reads were cleaned by removing adaptor sequences and low quality reads with ambiguous 'N'.
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Adaptor remover removes adaptor fragments from raw short read sequence data and outputs data to FASTA format.
For the RAD sequencing data, after removing adaptor-ligated and low quality reads, we assigned the remaining reads to MCU-5 or Siokra 1−4 based on the index sequences, and the sorted reads were then further separated based on the restriction sites of EcoRI, ApeKI, and SbfI.
Raw reads were cleaned by removing adaptors and low quality reads before assembly.
Prior to hybridization forward- and reverse-probes were digested for removing adaptors.
After removing adaptors and low quality reads, 134,985,444 clean reads were obtained from sequencing.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com