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Exact(7)
Reads < 40 bp were also discarded.
Reads shorter than 20 bp were also discarded.
Trimmed reads less than 15 bp were also discarded from further analysis, the remaining reads were used in subsequent assembly.
Subsequently, reads with a length of less than 24 bp were also discarded and the remaining reads were used for the assembly.
The ESTs were further tested for vector sequence contamination using NCBI VecScreen; ESTs of less than 300 bp were also discarded.
SNP loci with an additional SNP within 7 bp were also discarded (but see Additional file 3) to avoid possible artifacts of slight alignment errors.
Similar(53)
Probes showing hairpin structures of more than 3-bp length were also discarded.
Sequences less than 100 bp in length were also discarded.
Reads less than 15 bp after trim were also discarded, the remaining reads were used in subsequent assembly.
We only kept reads with distance between the beginning of the read and the next RE1 site equal to 20, 21 and 22 bp for condition A and equals to 21, 22 and 23 bp for condition B. Secondly, interactions involving fragments which have no restriction site for the secondary enzyme or a secondary site with a position located less than 20 bp from the first restriction site were also discarded.
Families which LTR size is shorter or close to 200 bp (Osr19, Osr44, Tos17, Osr20, Osr24, Osr43) were also discarded, because the filter could lead to an under-estimation of LTR copy number.
More suggestions(15)
bp were also observed
bp were also tested
bp were also estimated
bp were also classified
bp were also anchored
bp were also found
bp were also split
bp were also seen
bp were also investigated
bp were also removed
bp were also used
bp were also excluded
bp were also trimmed
bp were also sequenced
bp were also overestimated
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