Index of /public/onso/2024Q1/WGS/NIST_HG_Trio
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hg003/ 2024-02-28 14:43 -
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hg004/ 2024-02-21 18:24 -
README.txt 2024-02-29 08:43 2.7K
# PacBio Onso Whole Genome Sequencing of HG002, HG003, HG004 trio
## Legal disclaimer
All trademarks, trade names, or logos mentioned or used are the property of their respective owners.
## Sample provenance
The HG002, HG003 and HG004 samples were obtained from NIST (https://shop.nist.gov/ccrz__ProductDetails?sku=8392)
## Library prep
For PCR-free library preparation, genomic DNA from HG002, HG003, and HG004 samples were enzymatically fragmented, end-repaired, and A-tailed using Onso Fragmentation DNA Library Prep kit per manufacturer's instructions.
## Data
The HG002 trio data set contains both full length and adapter trimmed reads sequenced on a PacBio Onso instrument in San Diego, CA.
The libraries were sequenced with paired-end 2x150bp sequencing chemistry to the following approximate depths:
HG002 - 50X
HG003 - 30X
HG003.2 (replicate) - 45X
HG004 - 45X
Below is a brief description of the file contents:
HG002_Onso_R1.fastq.gz - read1 fastq containing untrimmed reads
HG002_Onso_R1_trimmed.fastq.gz - read1 fastq containing adapter trimmed reads
HG002_Onso_R2.fastq.gz - read2 fastq containing untrimmed reads
HG002_Onso_R2_trimmed.fastq.gz - read2 fastq containing adapter trimmed reads
HG003.2_Onso_R1_trimmed.fastq.gz - read1 fastq containing adapter trimmed reads
HG003.2_Onso_R2_trimmed.fastq.gz - read2 fastq containing adapter trimmed reads
HG003_Onso_R1.fastq.gz - read1 fastq containing untrimmed reads
HG003_Onso_R1_trimmed.fastq.gz - read1 fastq containing adapter trimmed reads
HG003_Onso_R2.fastq.gz - read2 fastq containing untrimmed reads
HG003_Onso_R2_trimmed.fastq.gz - read2 fastq containing adapter trimmed reads
HG004_Onso_R1.fastq.gz - read1 fastq containing untrimmed reads
HG004_Onso_R1_trimmed.fastq.gz - read1 fastq containing adapter trimmed reads
HG004_Onso_R2.fastq.gz - read2 fastq containing untrimmed reads
HG004_Onso_R2_trimmed.fastq.gz - read2 fastq containing adapter trimmed reads
### Adapter Trimming
Adapter trimming of the trimmed fastqs was perfomed using the cutadapt application (https://cutadapt.readthedocs.io/en/stable/) with the following command:
```
cutadapt \
-a ATCGATTCGTGCTTGTCCGTGGTACTCGGCA \
-A ATCGATTCGTGCTCGATGAACCGGGCGCTTA \
--overlap 8 \
-j 10 \
-o {output.fastq1} \
-p {output.fastq2} \
{input.fastq1} \
{input.fastq2}
```
### Alignment
Reads can be aligned to the a reference fasta (e.g. hg38 without alt contigs) using bwa-mem and indexed with samtools.
```
bwa mem -t24 -R {RG_TAG} {REFERENCE_FASTA} {input.fastq1} {input.fastq2} | \
samtools sort -@4 -o {output.bam}
samtools index {output.bam}
```
*Rev 2024-02-27*