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2
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659
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GATK not working when clone to VM
gatk
updated 10 months ago by ★ 2.2k • written 10 months ago by • 0
0
votes
6
replies
3.0k
views
How to extract alignments with 0 mismatch from sam or bam file by using samtools?
bam samtools sam
updated 12 months ago by • 0 • written 3.0 years ago by • 0
0
votes
0
replies
359
views
How to sync vcf file with the genome?
vcf
20 months ago by khanhlpbao • 0
2
votes
1
reply
406
views
Do I need to keep unmapped sequence on Variant calling?
bam variation unmapped
updated 21 months ago by 82k • written 21 months ago by • 0
0
votes
0
replies
350
views
Need help in explanation about article's binary hypothesis
nipt t-test
23 months ago by khanhlpbao • 0
0
votes
2
replies
527
views
Where to find and extract coordinates of common CNV and repetitive regions in human genome
cnv nipt
updated 2.2 years ago by 161k • written 2.2 years ago by • 0
2
votes
1
reply
952
views
Add or reveal read groups on .sam file aligned by BWA
gatk haplotypecaller
updated 2.5 years ago by 100k • written 2.5 years ago by • 0
1
vote
1
reply
543
views
LOSSES regression on python
python
updated 2.5 years ago by 3.2k • written 2.5 years ago by • 0
0
votes
1
reply
660
views
Need explain about number of mapped reads and total number reads
nipt
updated 2.5 years ago by 100k • written 2.5 years ago by • 0
0
votes
1
reply
1.1k
views
Comment: Comment: How convert reverse strain location to forward strain location?
2.6 years ago by khanhlpbao • 0
0
votes
3
replies
1.1k
views
How convert reverse strain location to forward strain location?
NIPT
updated 2.6 years ago by 100k • written 2.6 years ago by • 0
0
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1
reply
1.2k
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Comment: Comment: NIPT related tools & software
3.0 years ago by khanhlpbao • 0
0
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0
replies
3.0k
views
Comment: Comment: How to extract alignments with 0 mismatch from sam or bam file by using samtools
3.0 years ago by khanhlpbao • 0
0
votes
0
replies
3.0k
views
Comment: Comment: How to extract alignments with 0 mismatch from sam or bam file by using samtools
3.0 years ago by khanhlpbao • 0
0
votes
2
replies
3.8k
views
Comment: Comment: How to use seqff.r script (estimating fetal fraction)
3.0 years ago by khanhlpbao • 0
0
votes
0
replies
517
views
Repeats that affects NIPT results
NIPT NGS
3.0 years ago by khanhlpbao • 0
0
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0
replies
1.3k
views
Comment: Comment: Why GC content is important on NIPT results?
3.1 years ago by khanhlpbao • 0
0
votes
1
reply
1.3k
views
Comment: Comment: Why GC content is important on NIPT results?
3.1 years ago by khanhlpbao • 0
1
vote
4
replies
1.3k
views
Why GC content is important on NIPT results?
NGS NIPT Sequencing
3.1 years ago by khanhlpbao • 0
0
votes
1
reply
837
views
Comment: Comment: Trim alignment from .sam file based on a specific tab-delimiter .bed file
3.1 years ago by khanhlpbao • 0
0
votes
3
replies
837
views
Trim alignment from .sam file based on a specific tab-delimiter .bed file
sam
updated 3.1 years ago by 161k • written 3.1 years ago by • 0
2
votes
1
reply
1.2k
views
BWA-MEM or BWA-ALN + BWA-SAMSE for MGI sequencing
bwa ali sequencing
updated 3.1 years ago by 82k • written 3.1 years ago by • 0
0
votes
1
reply
20k
views
Comment: C: Creating chromosome karyotype plot with R and ggplot2
3.3 years ago by khanhlpbao • 0
0
votes
0
replies
469
views
Programs for analyze microarray results
genome
3.3 years ago by khanhlpbao • 0
0
votes
0
replies
664
views
NIPTeR Error in splitted_reads[[2]] : subscript out of bounds
NIPTeR alignment
3.4 years ago by khanhlpbao • 0
0
votes
1
reply
3.8k
views
Answer: A: How to use seqff.r script (estimating fetal fraction)
3.4 years ago by khanhlpbao • 0
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