I need to know how I can convert personal genome SNP format (pgSnp) to bam/bai and to fastq, and vice versa. The only tools relevant to pgSnp on galaxy convert VCF and CG mastervar to pgSNP. If anyone can help with the above, that would be awesome. Thanks in advance.
Unconfigured Ad
Collapse
X
-
BUMP! Anyone?
I've stumbled upon this program which I think might be relevant to what I'm trying to do. Let me know if anyone has any input:
GenomeGems performs simple comparisons using graphs and tables of data produced from different samples, and a wide and detailed visualization of the Deep Sequencing pre-processed data. GenomeGems integrates well with the University of California Santa Cruz (UCSC) Genome Browser for the purpose of SNP visualization within investigated chromosomes. This function is made possible by development of algorithms for conversion of a pre-processed input data to a Personal Genome SNP data format (PgSNP) , which can be viewed and further analyzed using UCSC . In addition to all of this, GenomeGems suggests a few useful external databases for further SNP investigation.
Thanks in advance.
-
-
doesn't look like you can
pgSnp looks like it just contains information on SNPs; it's what you might get after aligning a fasta or fastq file of sequencing reads to produce a BAM file and then analyzing the BAM file with a tool like freebayes or mpileup to find differences between your sequencing reads and the reference sequence. You can't go back from pgSnp to the other formats because it's a summary of them. You need to find the original datafiles that were used to generate your pgSnp files.
Comment
-
-
Thanks for the input! Do you have any advice on getting BAM and fastq > pgSnp?Originally posted by arolfe View PostpgSnp looks like it just contains information on SNPs; it's what you might get after aligning a fasta or fastq file of sequencing reads to produce a BAM file and then analyzing the BAM file with a tool like freebayes or mpileup to find differences between your sequencing reads and the reference sequence. You can't go back from pgSnp to the other formats because it's a summary of them. You need to find the original datafiles that were used to generate your pgSnp files.
Comment
-
Latest Articles
Collapse
-
by SEQadmin2
Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.
The systematic characterization of the human proteome has...-
Channel: Articles
07-20-2026, 11:48 AM -
-
by SEQadmin2
Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
...-
Channel: Articles
07-09-2026, 11:10 AM -
-
by SEQadmin2
Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.
There is no single reason why many patients don’t respond to treatment as expected. Cancer is...-
Channel: Articles
07-08-2026, 05:17 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, 07-20-2026, 11:10 AM
|
0 responses
14 views
0 reactions
|
Last Post
by SEQadmin2
07-20-2026, 11:10 AM
|
||
|
Started by SEQadmin2, 07-13-2026, 10:26 AM
|
0 responses
31 views
0 reactions
|
Last Post
by SEQadmin2
07-13-2026, 10:26 AM
|
||
|
Started by SEQadmin2, 07-09-2026, 10:04 AM
|
0 responses
42 views
0 reactions
|
Last Post
by SEQadmin2
07-09-2026, 10:04 AM
|
||
|
Started by SEQadmin2, 07-08-2026, 10:08 AM
|
0 responses
28 views
0 reactions
|
Last Post
by SEQadmin2
07-08-2026, 10:08 AM
|
Comment