reads_table: Sample Read Sequences
In Benji-Wagner/SequenceMapper: Map Reads to Reference Barcodes
Description
Usage
Format
Source
Description
A dataset containing identifiers, called bases, and Phred Quality Scores of 10000 reads.
Usage
1
Format
A data frame with 10000 rows and 3 variables:
- Read_ID
Unique Identifier containing the machine name, the run ID, the flowcell ID,
the x-coordinate of the cluster within the tile,
the y-coordinate of the cluster within the tile,
and a Y indicator if the read is filtered or N otherwise followed by the control bits
- Called_Read
DNA Sequences of length 18
- Phred_Score
ASCII-encoded probability of sequencing error of length 18
Source
Randomly generated sequences
Benji-Wagner/SequenceMapper documentation built on June 6, 2019, 1:08 p.m.
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Description Usage Format Source
Description
A dataset containing identifiers, called bases, and Phred Quality Scores of 10000 reads.
Usage
1 |
Format
A data frame with 10000 rows and 3 variables:
- Read_ID
Unique Identifier containing the machine name, the run ID, the flowcell ID, the x-coordinate of the cluster within the tile, the y-coordinate of the cluster within the tile, and a Y indicator if the read is filtered or N otherwise followed by the control bits
- Called_Read
DNA Sequences of length 18
- Phred_Score
ASCII-encoded probability of sequencing error of length 18
Source
Randomly generated sequences
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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