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Measure | Value |
---|---|
Filename | 5T.fastq |
File type | Conventional base calls |
Encoding | Sanger / Illumina 1.9 |
Total Sequences | 208049 |
Sequence length | 40-829 |
%GC | 45 |
Sequence | Count | Percentage | Possible Source |
---|---|---|---|
CTAATACGACTCACTATAGGGCAAGCAGTGGTATCAACGCAGAGTACGCG | 42476 | 20.416344226600465 | No Hit |
CTAATACGACTCACTATAGGGCAAGCAGTGGTATCAACGCAGAGTTACTT | 1244 | 0.5979360631389721 | No Hit |
Measure | Value |
---|---|
Filename | 5T.fastq |
File type | Conventional base calls |
Encoding | Sanger / Illumina 1.9 |
Total Sequences | 845357 |
Sequence length | 40-1596 |
%GC | 43 |
Sequence | Count | Percentage | Possible Source |
---|---|---|---|
CTAATACGACTCACTATAGGGCAAGCAGTGGTATCAACGCAGAGTACGCG | 237291 | 28.06991602364445 | No Hit |
CTAATACGACTCACTATAGGGCTGTGACTAGTATGTTGAGTCCTGTAAGT | 11071 | 1.3096242179339617 | No Hit |
Barcelona![]() |
Sevilla![]() |
208049 total reads. 189211 (91%) input to Newbler v2.5p1-internal-10Jun23-1. numAlignedReads = 111377, 58.86%; numAlignedBases = 33876333, 57.30%; inferredReadError = 1.57%, 532790; numberAssembled = 88957; (47%) numberPartial = 22297; numberSingleton = 73790; (39%) numberRepeat = 186; numberOutlier = 3554; numberTooShort = 427; numberOfIsotigs = 4423; avgContigCnt = 2.0; largestContigCnt = 16; numberWithOneContig = 2812; numberOfBases = 2586937; avgIsotigSize = 584; N50IsotigSize = 587; largestIsotigSize = 3141; |
845357 total reads. 835080 (99%) input to Newbler v2.6. numAlignedReads = 589924, 70.64%; numAlignedBases = 300516134, 69.44%; inferredReadError = 0.91%, 2744346; numberAssembled = 504405; (60%) numberPartial = 85416; numberSingleton = 214098; (26%) numberRepeat = 444; numberOutlier = 22477; numberTooShort = 8240; numberOfIsotigs = 17939; avgContigCnt = 1.9; largestContigCnt = 14; numberWithOneContig = 10968; numberOfBases = 22496014; avgIsotigSize = 1254; N50IsotigSize = 1328; largestIsotigSize = 8287; |
Barcelona![]() |
Sevilla![]() |
185847 reads mapped to hg19 (89%). Genomic distribution of aligned reads
![]() Fraction of reads aligned inside targeted regions vs. min % sequence identity threshold
![]() |
826262 reads mapped to hg19 (98%). Genomic distribution of aligned reads
![]() Fraction of reads aligned inside targeted regions vs. min % sequence identity threshold ![]() |