- taking trim trim (remove 4bp 5' and <90bp length)
and "Removing Duplicates"

De novo assembly of 8 libraries without duplicates


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cgigas_tag-seq_8_95.pdf
cgigas_tag-seq_8_95_a.csv<- stat table


SAM format

http://eagle.fish.washington.edu/cnidarian/cgigas_tag-seq_8_95.sam


Fasta of contigs

http://eagle.fish.washington.edu/cnidarian/cgigas_tag-seq_8_95.fa


--
Assembly with different parameters (stricter)



cgigas_tag-seq_9_98.pdf

cgigas_tag-seq_9_98.csv<-- stat table

http://eagle.fish.washington.edu/cnidarian/cgigas_tag-seq_9_98.sam

http://eagle.fish.washington.edu/cnidarian/cgigas_tag-seq_9_98.fa


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subset of denovo

for denovo smaller than 200 bp - (went form 72k to 67k)

Contig sequences from 9_98 without duplicates de novo assembly _200.fa

test.fa.masked

note that this is assembly was done with duplicates removed, thus singlets (those that did not assemble) could be important
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Running RNA-seq on this backbone