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Most importantly, more comprehensive genome-scale analysis using array-based platforms or next-generation sequencing will be needed [ 127].
Further studies with more crypts and sequences will be needed to distinguish between these possibilities.
It is more than probable that arrays for 50 100 DNA sequences will be needed for some clinical applications.
In particular, more sampling of Potamocoridae, Micronectidae and Diaprepocoridae (Hemiptera: Nepomorpha) mt-genome sequences will be needed for a thorough analysis of the major groups within Nepomorpha.
Therefore, more sequence data will be needed to confirm that the 31 singleton sequences are correct.
Although illegitimate V(D J recombination may be responsible for creating CDKN2A deletions in acute lymphoblastic leukemia, more breakpoint sequence data will be needed for other types of cancers to delineate the molecular mechanisms [37], [38], [47], [48].
This implies that more complete sequence data will be needed to obtain a reliable comparison of the size of the GC-poorest LHGRs between the pig and human genomes.
This implies that more complete sequence data will be needed in order to obtain reliable assessments of the GC-poorest isochore size of medaka, stickleback (and also of zebrafish, opossum and chimpanzee).
More accommodation will be needed.
If the slowdown is serious, more cuts will be needed.
More research will be needed to confirm these findings.
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