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Dear Jim,
Thank you for the amazing IGV notebook tool.
I recently wanted to visualize some alignments (in BAM format) using IGV notebook against the T2T genome from RefSeq (GCF_009914755.1). I tried using both relative paths (code provided below) and absolute paths but none of them was able to show alignments. Could you please advise if there is any incorrect usage with the following implementations? Many thanks in advance!
Note: Jupyter server was started under the directory /paedyl01/disk1/louisshe/. Working directory is /paedyl01/disk1/louisshe/work/common. The version of igv-notebook I am using us 0.5.2.
(Relative paths)
import igv_notebook
igv_notebook.init()
# Browse a local FASTA genome
b = igv_notebook.Browser(
{
"reference": {
"id": "T2T-CHM13v2.0",
"name": "T2T",
"fastaURL": "ref/T2T/GCF_009914755.1/GCF_009914755.1_T2T-CHM13v2.0_genomic.fa",
"indexURL": "ref/T2T/GCF_009914755.1/GCF_009914755.1_T2T-CHM13v2.0_genomic.fa.fai"
},
"locus": "NC_060928.1:193,432,000-193,554,000"
}
)
# Load alignment data
b.load_track(
{
"name": "HG02723 PacBio HiFi",
"url": "out/D4Z4_HG02723_test/PacBio_HiFi/merged_mapped.sorted.bam",
"indexURL": "out/D4Z4_HG02723_test/PacBio_HiFi/merged_mapped.sorted.bam.bai",
"format": "bam",
"type": "alignment"
}
)
b.zoom_in()(absolute paths)
import igv_notebook
igv_notebook.init()
# Browse a local FASTA genome
b = igv_notebook.Browser(
{
"reference": {
"id": "T2T-CHM13v2.0",
"name": "T2T",
"fastaURL": "/paedyl01/disk1/louisshe/ref/T2T/GCF_009914755.1/GCF_009914755.1_T2T-CHM13v2.0_genomic.fa",
"indexURL": "/paedyl01/disk1/louisshe/ref/T2T/GCF_009914755.1/GCF_009914755.1_T2T-CHM13v2.0_genomic.fa.fai"
},
"locus": "NC_060928.1:193,432,000-193,554,000"
}
)
# Load alignment data
b.load_track(
{
"name": "HG02723 PacBio HiFi",
"url": "/paedyl01/disk1/louisshe/out/D4Z4_HG02723_test/PacBio_HiFi/merged_mapped.sorted.bam",
"indexURL": "/paedyl01/disk1/louisshe/out/D4Z4_HG02723_test/PacBio_HiFi/merged_mapped.sorted.bam.bai",
"format": "bam",
"type": "alignment"
}
)
b.zoom_in()Metadata
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