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1.3k
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GATK not working when clone to VM
gatk
updated 2.3 years ago by ★ 2.5k • written 2.3 years ago by • 0
1
vote
6
replies
4.3k
views
How to extract alignments with 0 mismatch from sam or bam file by using samtools?
bam samtools sam
updated 2.5 years ago by • 0 • written 4.4 years ago by • 0
0
votes
0
replies
522
views
How to sync vcf file with the genome?
vcf
3.2 years ago by khanhlpbao • 0
2
votes
1
reply
684
views
Do I need to keep unmapped sequence on Variant calling?
bam variation unmapped
updated 3.2 years ago by 89k • written 3.2 years ago by • 0
0
votes
0
replies
605
views
Need help in explanation about article's binary hypothesis
nipt t-test
3.4 years ago by khanhlpbao • 0
0
votes
2
replies
828
views
Where to find and extract coordinates of common CNV and repetitive regions in human genome
cnv nipt
updated 3.6 years ago by 166k • written 3.6 years ago by • 0
2
votes
1
reply
1.5k
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Add or reveal read groups on .sam file aligned by BWA
gatk haplotypecaller
updated 3.9 years ago by 103k • written 3.9 years ago by • 0
1
vote
1
reply
843
views
LOSSES regression on python
python
updated 4.0 years ago by 3.4k • written 4.0 years ago by • 0
0
votes
1
reply
900
views
Need explain about number of mapped reads and total number reads
nipt
updated 4.0 years ago by 103k • written 4.0 years ago by • 0
0
votes
1
reply
1.6k
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Comment: Comment: How convert reverse strain location to forward strain location?
4.1 years ago by khanhlpbao • 0
0
votes
3
replies
1.6k
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How convert reverse strain location to forward strain location?
NIPT
updated 4.1 years ago by 103k • written 4.1 years ago by • 0
0
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1
reply
1.6k
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Comment: Comment: NIPT related tools & software
4.4 years ago by khanhlpbao • 0
0
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0
replies
4.3k
views
Comment: Comment: How to extract alignments with 0 mismatch from sam or bam file by using samtools
4.4 years ago by khanhlpbao • 0
0
votes
0
replies
4.3k
views
Comment: Comment: How to extract alignments with 0 mismatch from sam or bam file by using samtools
4.4 years ago by khanhlpbao • 0
0
votes
2
replies
5.3k
views
Comment: Comment: How to use seqff.r script (estimating fetal fraction)
4.4 years ago by khanhlpbao • 0
0
votes
0
replies
688
views
Repeats that affects NIPT results
NIPT NGS
4.5 years ago by khanhlpbao • 0
0
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0
replies
2.0k
views
Comment: Comment: Why GC content is important on NIPT results?
4.5 years ago by khanhlpbao • 0
0
votes
1
reply
2.0k
views
Comment: Comment: Why GC content is important on NIPT results?
4.5 years ago by khanhlpbao • 0
1
vote
4
replies
2.0k
views
Why GC content is important on NIPT results?
NGS NIPT Sequencing
4.5 years ago by khanhlpbao • 0
0
votes
1
reply
1.2k
views
Comment: Comment: Trim alignment from .sam file based on a specific tab-delimiter .bed file
4.6 years ago by khanhlpbao • 0
0
votes
3
replies
1.2k
views
Trim alignment from .sam file based on a specific tab-delimiter .bed file
sam
updated 4.6 years ago by 166k • written 4.6 years ago by • 0
2
votes
1
reply
1.8k
views
BWA-MEM or BWA-ALN + BWA-SAMSE for MGI sequencing
bwa ali sequencing
updated 4.6 years ago by 89k • written 4.6 years ago by • 0
0
votes
1
reply
22k
views
Comment: C: Creating chromosome karyotype plot with R and ggplot2
4.7 years ago by khanhlpbao • 0
0
votes
0
replies
617
views
Programs for analyze microarray results
genome
4.7 years ago by khanhlpbao • 0
0
votes
0
replies
893
views
NIPTeR Error in splitted_reads[[2]] : subscript out of bounds
NIPTeR alignment
4.9 years ago by khanhlpbao • 0
0
votes
1
reply
5.3k
views
Answer: A: How to use seqff.r script (estimating fetal fraction)
4.9 years ago by khanhlpbao • 0
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